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OTC products · Product label record

Hydrocortisone drug information

HYDROCORTISONE
Amazon.com Services LLC · TOPICAL

Product NDC: 72288-469

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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 nameHYDROCORTISONE
Labeler / manufacturerAmazon.com Services LLC
RouteTOPICAL
Drug classCorticosteroid
Product NDC72288-469
Label effective date2026-08-25

Official product label reference

Hydrocortisone — Amazon.com Services LLC

This page contains 12 source sections for HYDROCORTISONE, topical route. Label set 5f87d7fb-f258-48b0-8b60-1055e22ebd71, version 2.

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 relieves itching associated with minor skin irritations, rashes, and inflammation due to eczema • other uses of this product should be only under the advice and supervision of a doctor

Purpose

Purpose Anti-itch
Dosage and administration — label text
Directions • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor
Warnings
Warnings For external use only Do not use • for the treatment of diaper rash. Consult a doctor. When using this product • avoid contact with eyes • do not use more than directed unless told to do so by a doctor Stop use and ask a doctor if • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
Active ingredient
Active ingredient Hydrocortisone 1%
Do not use
Do not use • for the treatment of diaper rash. Consult a doctor.
While using this medicine
When using this product • avoid contact with eyes • do not use more than directed unless told to do so by a doctor
Ask a doctor before use
Stop use and ask a doctor if • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
Unclassified section
Other information • store at 20-25°C (68-77°F) • contents filled by weight, not volume
Inactive ingredient
Inactive ingredients aloe barbadensis leaf juice, avena sativa (oat) kernel extract, bisabolol, boswellia serrata gum, butyrospermum parkii (shea butter) extract, cetyl alcohol, dextrin, dimethicone, dipropylene glycol, edetate disodium, glycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, magnesium ascorbyl phosphate, maltodextrin, methyl gluceth-20, methylparaben, petrolatum, phenoxyethanol, polysorbate 60, propylparaben, purified water, retinyl palmitate, sodium citrate, tocopheryl acetate, zingiber officinale (ginger) root extract
Questions
Questions or comments? 1-800-719-9260

Official sources and product identifiers

Substances listed: HYDROCORTISONE

RxNorm identifiers: 103403

Package NDC codes

72288-469-00, 72288-469-25

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.