Otc - Active Ingredient
Hydrocortisone 1%
The following Structured Product Label (SPL) was submitted to the FDA by Walgreens for the product Walgreens Scalp Itch Relief (NDC 0363-1414). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - pregnancy or breast feeding, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Hydrocortisone 1%
Anti-itch liquid
Temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to: eczema, psoriasis, and seborrheic dermatitis. Other uses of this product should be only under the advice and supervision of a doctor.
For external use only. Use only as directed.
Flammable. Keep away from fire or flame.
Do not use for the treatment of diaper rash; consult a doctor if you are allergic to any ingredient in this product.
When using this product avoid contact with eyes, do not use more than directed unless told to by a doctor.
Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, do not use this or any other hydrocortisone product unless you have asked a doctor.
Ask a health professional before use.
If product is swallowed, get medical help or contact a Poison Control Center right away.
Adults and children 2 years of age and older:
Alcohol denat., water, propylene glycol, PEG-40/PPG-8 methylaminopropyl/hydroxypropyl dimethicone copolymer, glycerin, dipropylene glycol, menthol, disodium EDTA, aloe barbadensis leaf juice, isopropyl alcohol, melaleuca alternifolia (tea tree) leaf oil, tocopheryl acetate
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