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First Aid Beauty Face and Body Bestsellers Kit drug information

COLLOIDAL OATMEAL
The Procter & Gamble Manufacturing Company · TOPICAL

Product NDC: 84126-911

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameCOLLOIDAL OATMEAL
Labeler / manufacturerThe Procter & Gamble Manufacturing Company
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC84126-911
Label effective date2026-09-03

Official product label reference

First Aid Beauty Face and Body Bestsellers Kit — The Procter & Gamble Manufacturing Company

This page contains 11 source sections for COLLOIDAL OATMEAL, topical route. Label set 5a974dbf-84ac-5374-e063-6294a90a8da0, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

Purpose Skin Protectant
Dosage and administration — label text
Directions ​Apply as needed
Warnings
Warnings For external use only. If swallowed, get medical help or contact Poison Control Center right away. 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
Unclassified section
Drug Facts MADE IN USA FIRST AID BEAUTY LTD NEWTON, MA 02458 WWW.FIRSTAIDBEAUTY.COM
Active ingredient
Active ingredient Colloidal Oatmeal 0.5%
Child safety
If swallowed, get medical help or contact Poison Control Center right away.
While using this medicine
When using this product Do not get into eyes
Ask a doctor before use
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
Inactive ingredient
Inactive ingredients Water, stearic acid, glycerin, C12-15 alkyl benzoate, caprylic/capric triglyceride, glyceryl stearate SE, glyceryl stearate, cetearyl alcohol, dimethicone, squalane, butyrospermum parkii (shea) butter, phenoxyethanol, caprylyl glycol, xanthan gum, allantoin, sodium hydroxide, tetrasodium EDTA, chrysanthemum parthenium (feverfew) extract, camellia sinensis leaf extract, glycyrrhiza glabra (licorice) root extract, ceramide NP, eucalyptus globulus (eucalyptus) leaf oil
Questions
Questions: 888-FAB-3063

Official sources and product identifiers

RxNorm identifiers: 1654149

Package NDC codes

84126-911-01, 84126-203-11

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.