Mederma for Kids

ALLANTOIN TOPICAL HUMAN OTC DRUG

Mederma for Kids is an FDA drug label for the active ingredient ALLANTOIN manufactured by L. Perrigo Company administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260714.

Generic name
ALLANTOIN
Manufacturer
L. Perrigo Company
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
0113-4126
Application
M016
Label effective
20260714

About this product

Mederma for Kids is an FDA-registered drug product whose active ingredient is ALLANTOIN. It is labelled by L. Perrigo Company taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 0113-4126, application M016, label effective 20260714. It is one of 9 FDA drug label records sharing the active ingredient ALLANTOIN. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ALLANTOIN are most often described in connection with: temporarily protects, helps relieve, chapped cracked. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENT Allantoin 1%

Indications & Usage

USES • Temporarily protects and helps relieve chapped or cracked skin

Dosage & Administration

DIRECTIONS • Apply as needed

Warnings

WARNINGS • For external use only When using this product • Do not get into eyes Stop use and ask a doctor if • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days Do not use on • Deep or puncture wounds • Animal bites • Serious burns Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

More products with the same ingredient

ALLANTOIN

ADVANCED SILICONE SCAR

Yantai Aien Biotechnology Co., Ltd. View label

Calm and Heal Melting Balm

The Honest Company, Inc. View label

Cetaphil Baby Soothe and Protect Cream

Galderma Laboratories, L.P. View label

DeFlame

Noon Aesthetics M.R. Ltd View label

Drs. pharmacy Scar Cream

OL PHARMA TECH, LLC Drs PHARMACY View label

Mederma Advanced Scar

L. Perrigo Company View label

Mederma Advanced Scar

PMI Branded Pharmaceuticals, Inc. View label

How products containing ALLANTOIN compare

FDA lists 9 drug label records with ALLANTOIN as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — L. Perrigo Company 2
— — Galderma Laboratories, L.P. 1
— — Guangzhou Yapheon Health Industry Co., Ltd. 1
— — Noon Aesthetics M.R. Ltd 1
— — OL PHARMA TECH, LLC Drs PHARMACY 1

Recall and safety notices

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0912-2023 Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 36800-691-39), b)45-count cartons (NDC 36800-691-95), and 90-count cartons (NDC 36800-691-75), Distributed by: Topco Associates LLC, Elk Grove Village, IL 60007. L. Perrigo Company Class II Terminated 20230719
D-0910-2023 allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 11673-617-22), b)30-count cartons (NDC 11673-617-39), c)70-count cartons (NDC 11673-617-01), and d)150-count cartons (11673-617-47), Distributed by: Target Corporation, Minneapolis, MN 55403. L. Perrigo Company Class II Terminated 20230719
D-0909-2023 allergyrelief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)30-count cartons (NDC 56062-847-39); and b) 45-count cartons (NDC 56062-847-95), Distributed by: Publix Super Markets, Inc., 3300 Publix Corporate Parkway, Lakeland, FL 33811. L. Perrigo Company Class II Terminated 20230719
D-0906-2023 allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 79481-0847-0), b)30-count cartons (NDC 79481-0847-1), and c) 45-count cartons (NDC 79481-0847-2), Distributed by: MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544. L. Perrigo Company Class II Terminated 20230719
D-0903-2023 Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 69842-0914-39 L. Perrigo Company Class II Terminated 20230719

Frequently asked questions

What is Mederma for Kids used for?
USES • Temporarily protects and helps relieve chapped or cracked skin

Who makes Mederma for Kids?
L. Perrigo Company is the labeler of record for Mederma for Kids. 9 FDA label records share the active ingredient ALLANTOIN, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Mederma for Kids come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Mederma for Kids prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing ALLANTOIN?
Yes. 9 FDA drug label records list ALLANTOIN as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Mederma for Kids been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.