The FDA oversees all food and drug products. Since Colic-Ease is a dietary supplement, it does not fall into either of these categories. However, in 1994 the FDA set up guidelines for dietary supplements, including labeling requirements, and created the Dietary Supplement Health Education Act (DSHEA). Colic-Ease follows all of DSHEA's guidelines.

You can use Colic-Ease again when introducing new foods into your baby's diet that may cause gas pains. It is also effective for adults experiencing heartburn, bloating, nausea or indigestion. Adult dose is 4 tablespoons.

Only the Colic-Ease gripe water is a purely herbal remedy consisting of five essential oils. Each of these oils contain properties that when combined, allow Colic-Ease to address the broadest range of symptoms. Conversely, other gripe water brands rely on the effect of non-herbal ingredients (i.e. sodium bicarbonate or charcoal) in their formulas. You can read more about why we don't use sodium bicarbonate or charcoal for infants in this FAQ section.

EACH ONE OF THE HERBS in the Colic-Ease formula is listed on the FDA's GRAS, Generally Recognized As Safe, list. For a detailed description of the full benefits of each herb individually please visit our ingredients page

Yes, at Colic-Ease, Inc. we are dedicated to providing our customers with a gripe water product of unsurpassed quality. The ingredients in Colic-Ease gripe water have met stringent requirements before being approved for use in our formula. Prior to being released for shipment, testing is done on every new production batch to confirm the accuracy of the formulation's ingredients.

In hiccups, the diaphragm spasms, causing pain and discomfort. The Caraway Seed Oil in Colic-Ease is derived from a group of plants that help alleviate these painful spasms. During teething, babies can cry excessively, taking in air. The Dillweed Seed Oil in Colic-Ease has an antifoaming action which dispels flatulence (gas) that is formed by this excessive air intake.

We accept Visa, Visa debit, MasterCard and MasterCard debit online 24 hours a day. You can give us a call to place a phone order at 516-520-7280.

Colic-Ease may be stored up to 3 years if unopened. Once opened, it can be stored safely and remain effective for six months when kept at room temperature, out of direct sunlight.

We get positive feedback about both methods, try each one and you will be able to see which method is working best for your baby.

While there are many unapproved substances used to sclerose spider veins, hypertonic saline is the only agent approved by the FDA. Kalologie Skincare uses hypertonic saline for all sclerotherapy treatments.

We strongly advise parents to consult with their baby's pediatrician before using Colic-Ease in combination with any over-the-counter products or prescriptions. If you have additional questions, please contact us using our contact form.

The Food & Drug Administration does not have an approval process for any nutritional supplements, only perscription medications. However, Flexcin is manufactured in a FDA inspected and approved facility.

The U. S. Congress passed the Dietary Supplement Health and Education Act (DSHEA) of 1994 which spells out the regulations as they apply to dietary supplements.

The price of the test is $200, including shipping costs. Payment can be made by any major credit card by the individual or by the ordering physician or clinic, by including the card details on the test request form. Samples submitted anonymously must be accompanied by a valid credit card number from the respective doctor or affiliated health care institution.

Currently, non-prescription nutritional supplements do not require FDA approval. However, BioVitale's Digestive Enzyme Complex is manufactured in a FDA monitored and approved facility under the highest quality control standards.

a dietary supplement, XanGo is considered a food, and does not require FDA approval. The FDA does not offer opinions on or approval of dietary supplements. Independent laboratory testing confirms the safety and purity of all components of XanGo Juice.

The anti-pathogenic and germicidal properties of the silver oxide in Safe Lips has been tested by 14 reputable and independent Contract Research Organizations (CROs). Countless individuals have contacted us with their very positive feedback, declaring the Safe Lips was the major factor in returning them to healthy skin. Furthermore, we have a very liberal return policy where customer satisfaction is 100% guaranteed, and yet we have experienced very few returns.

In 1998, Herceptin was approved for the treatment of HER2+ metastatic breast cancer. In 2006, the FDA approved Herceptin for the adjuvant treatment of patients with HER2+, node-positive breast cancer.

Ans : Since Gourdin is a dietary supplement and NOT a drug, it doesn't necessarily need to be approved by FDA / MHRA (UK). It is used as a health food without a doctor's prescription. We are, however, refining it and working toward applying for FDA / MHRA (UK) approval. We assure you that this in no way reduces the qualities or efficacy of the supplement. We have received a tremedous positive response from our users. And those who still have doubts, we have designed special trial packs for them.

Simethicone, the active ingredient in Phazyme® is the only FDA approved antiflatulent drug. Simethicone meets the OTC Monograph as a safe and effective antiflatulent agent and is regulated as an over the counter drug by the FDA.

Yes, most of our users of the Quit Smoking Support System reported that they managed to stop smoking and no longer experienced cravings or withdrawal symptoms. Few smoking cessation products out there can make such similar claims in efficacy, ease, and successfulness.

GHR Platinum is an all-natural supplement and does not fall into the approval jurisdiction of the FDA.

ECP is approved by the FDA for the treatment of Angina and Congestive Heart Failure. It has undergone rigorous clinical trials at leading universities around the country and ECP has been the subject of scientific studies published in leading medical journals.

The US Food and Drug Administration (FDA) does not approve or disapprove of any kind of dietary supplements, such as Revivol ™, since it is not within their responsibility. The FDA only approves or disapproves of pharmaceutical drugs, which Revivol™ is not.

ZymaDerm is 'FDA Compliant' and conforms to the standards of the Homeopathic Pharacopeia of the United States (HPUS), a compendium recognized as both official and authoritative by the FDA. Each of the ingredients in ZymaDerm is stated in the Pharmacopeia to be useful as an aid in the treatment of skin rash conditions. If a drug-free agent is listed in the HPUS for treating certain conditions, a product containing that agent may be marketed for those conditions without specific FDA approval.

Our entire service has been scientifically reviewed for safety and effectiveness by the U.S. Food and Drug Administration (FDA). FDA granted Home Access Health nationwide clearance to market its service on April 28, 1999. The Home Access at-home telemedicine Hepatitis C counseling and testing service is the ONLY such service available in the United States approved by the U.S. Food and Drug Administration.

Infantile colic was first described as indigestion. While different diagnostic criteria have emerged since then, there has never been complete agreement on what colic is, what causes it, or how to treat it. The most widely accepted definition of colic today is "unexplainable and uncontrollable crying in babies from 0 to 3 months old, more than 3 hours a day, more than 3 days a week for 3 weeks or more, usually in the afternoon and evening hours."