KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery

KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery is an FDA-registered drug product whose active ingredient is COLLOIDAL OATMEAL. It is labelled by LOreal USA Products Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 49967-571, application M016, label effective 20260529. It is one of 27 FDA drug label records sharing the active ingredient COLLOIDAL OATMEAL. 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.

Across FDA labelling, products containing COLLOIDAL OATMEAL are most often described in connection with: temporarily protects, helps relieve, minor skin, itching due, rashes eczema, poison ivy, oak sumac, insect bites. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily protects and helps relieve minor skin irritation and itching due to: rashes eczema poison ivy, oak, or sumac insect bites

Directions apply as needed

Warnings For external use only

FDA lists 27 drug label records with COLLOIDAL OATMEAL 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.

What is KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery used for?
Uses temporarily protects and helps relieve minor skin irritation and itching due to: rashes eczema poison ivy, oak, or sumac insect bites

Who makes KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery?
LOreal USA Products Inc is the labeler of record for KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery. 27 FDA label records share the active ingredient COLLOIDAL OATMEAL, 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 KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery 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 KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery 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 COLLOIDAL OATMEAL?
Yes. 27 FDA drug label records list COLLOIDAL OATMEAL 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 KIEHLS SINCE 1851 Ultra Facial Meltdown Recovery 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.