Active Ingredient
Hydrocortisone 1%
The following Structured Product Label (SPL) was submitted to the FDA by H E B for the product Hydrocortisone (NDC 37808-973). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Hydrocortisone 1%
Anti-itch
For external use only
If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
aloe barbadensis leaf juice, aluminum sulfate, calcium acetate, cetearyl alcohol, cetyl alcohol, cholecalciferol, dextrin, glycerin, isopropyl palmitate, light mineral oil, maltodextrin, methylparaben, propylene glycol, propylparaben, purified water, retinyl palmitate, sodium cetearyl sulfate, sodium lauryl sulfate, tocopherol, white petrolatum, white wax, zea mays (corn) oil
1-800-719-9260
Compare to active ingredient in Cortizone-10® Plus
Maximum Strength
1% Hydrocortisone Cream
ANTI-ITCH CREAM
Plus 10 Moisturizers
Maximum Strength
1% Hydrocortisone Cream
ANTI-ITCH CREAM
Plus 10 Moisturizers
NET WT. 1 OZ (28g)
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