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OTC products · Product label record

MedPride drug information

HYDROCORTISONE
Shield Line LLC · TOPICAL

Product NDC: 52410-3050

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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 / manufacturerShield Line LLC
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC52410-3050
Label effective date2026-08-18

Official product label reference

MedPride — Shield Line LLC

This page contains 11 source sections for HYDROCORTISONE, topical route. Label set 2f15d3b3-d1e6-4742-9eac-f956c0ffbba4, version 11.

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 ■ for temporary relief of minor skin irritations, itching and rashes due to eczema, insect bites, poison ivy, poison oak, poison sumac, soaps, detergents, cosmetics, jewelry, and for external genital, feminine and anal itching. 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 over 2 years of age ■ apply evenly to affected area no more than 3 to 4 times daily ■ children under 2 years of age ■ do not use, consult a doctor ■ adults and children over 2 years of age ■ apply evenly to affected area no more than 3 to 4 times daily ■ children under 2 years of age ■ do not use, consult a doctor ■ Adults ■ when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly ■ gently dry, patting or blotting with bathroom tissue or soft cloth before applying ■ apply externally to the area up to 6 times a daily or after a bowel movement ■ after application discard pad ■ do not flush in toilet
Warnings
Warnings For external use only
Active ingredient
Active Ingredient Hydrocortisone Acetate USP (1% w/w)
Do not use
Do not use ■ in the eyes ■ for diaper rash ■ if you have vaginal discharge ■ more than the recommended dosage
Ask a doctor before use
Ask a doctor before use ■ if you are pregnant or breast feeding
When to stop use and seek help
Stop use and ask a doctor if ■ the condition worsens, or if symptoms persist for more than 7 days or clear up and occur again wihin a few days
Child safety
Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away
Unclassified section
Other information ■ store at 20-25C (68-77F) ■ avoid excessive heat and humidity
Inactive ingredient
Inactive Ingredients cetostearyl alcohol, chlorocresol, ceteth-20, edetate disodium, liquid paraffin, propylene glycol, purified water, sodium metabisulphite, White white soft paraffin

Official sources and product identifiers

Substances listed: HYDROCORTISONE ACETATE

RxNorm identifiers: 1043690

Package NDC codes

52410-3050-2, 52410-3050-3, 52410-3050-6

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.