MUSTELA Diaper Rash 1 2 3
MUSTELA Diaper Rash 1 2 3 is an FDA drug label for the active ingredient ZINC OXIDE manufactured by Expanscience Laboratories d/b/a Mustela 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 20260824.
- Generic name
- ZINC OXIDE
- Manufacturer
- Expanscience Laboratories d/b/a Mustela
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 64768-2292
- Application
- M016
- Label effective
- 20260824
About this product
MUSTELA Diaper Rash 1 2 3 is an FDA-registered drug product whose active ingredient is ZINC OXIDE. It is labelled by Expanscience Laboratories d/b/a Mustela taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 64768-2292, application M016, label effective 20260824. It is one of 404 FDA drug label records sharing the active ingredient ZINC OXIDE. 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 ZINC OXIDE are most often described in connection with: diaper rash, helps treat, protects minor, skin irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Helps treat and prevent diaper rash Protects minor skin irritation associated with diaper rash and helps seal out wetness
Dosage & Administration
Directions Change wet and soiled diapers promptly, cleanse the diaper area, and allow to dry. Apply cream liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.
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 Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
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View labelHow products containing ZINC OXIDE compare
FDA lists 404 drug label records with ZINC OXIDE 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 form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Ilia, Inc. | 30 |
| — | — | COSMAX USA, CORP | 24 |
| — | — | Colorescience | 16 |
| — | — | Allure Labs Inc | 9 |
| — | — | Raw Elements LLC | 9 |
Frequently asked questions
What is MUSTELA Diaper Rash 1 2 3 used for?
Uses Helps treat and prevent diaper rash Protects minor skin irritation associated with diaper rash and helps seal out wetness
Who makes MUSTELA Diaper Rash 1 2 3?
Expanscience Laboratories d/b/a Mustela is the labeler of record for MUSTELA Diaper Rash 1 2 3. 404 FDA label records share the active ingredient ZINC OXIDE, 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 MUSTELA Diaper Rash 1 2 3 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 MUSTELA Diaper Rash 1 2 3 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 ZINC OXIDE?
Yes. 404 FDA drug label records list ZINC OXIDE 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 MUSTELA Diaper Rash 1 2 3 been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
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.