Otc - Active Ingredient
Hydrocortisone 1.0%
Cvs Maximum Strength Anti-itch Cream
FDA Label NDC 69842-485
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Health for the product Cvs Maximum Strength Anti-itch Cream (NDC 69842-485). 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, otc - when using, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Anti-itch
Indications & Usage
Temporarily relieves external feminine itching
Otc - When Using
Avoid contact with the eyes
Otc - Do Not Use
If you are allergic to any of the ingredients
Otc - Stop Use
Stop use and ask the doctor if :
- conditions worsen
- symptoms last ore than 7 days, or clear up and occur again within a few days
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison control center right away.
Dosage & Administration
- Adults and children 12 years and over: Apply to the external vaginal area more than 3 times a day
- Children under 12 years: Consult a doctor
Other Safety Information
Store at 20-25 C (68-77 F)
Inactive Ingredient
aloe vera, Ascorbic acid, Cetyl alcohol, Citric acid, Glyceryl stearate, Mineral oil, PEG-100 Stearate, PEG-150 Distearate, Petrolatum, Phenoxyethanol, Polycarbophil, Propylene Glycol, Purified Water, Sodium citrate, Stearyl alcohol, Vitamin A palmitate, Vitamin E acetate, Xanthan Gum.
* Please review the disclaimer below.
