Active Ingredient
Hydrocortisone, USP 0.5%
Anti-itch Feminine Care Cream
FDA Label NDC 80489-103
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ol Pharma Tech, Llc Drs Pharmacy for the product Anti-itch Feminine Care (NDC 80489-103). 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, diretions, stop use and ask a doctor if, keep out of reach of children, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-itch
Uses
For temporary external feminine itching
Warnings
For External Use Only
Avoid Contact with eyes
Diretions
Adults and children 12 years and older Apply to external vaginal area not more than 3 to 4 times a day
Children under 12 years Consult a doctor
Stop Use And Ask A Doctor If
- you have a vaginal discharge. Consult a physician.
- condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again in a few days.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Other Information
- store at 20°-25°C (68°-77°F)
Inactive Ingredient
cetostearyl alcohol, sodium cetostearyl sulfate, stearic acid, trolamine, decyl oleate, propylene glycol, water, methyl paraben, propyl paraben, EDTA, vitamin E
Questions
www.drspharmacyusa.com
* Please review the disclaimer below.
