Otc - Active Ingredient
Active Ingredient
Hydrocortisone 1%
The following Structured Product Label (SPL) was submitted to the FDA by Budpak Inc. for the product Budpak Anti-itch (NDC 27293-017). 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 - do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Active Ingredient
Hydrocortisone 1%
Purpose
Anti-itch
Uses
for the temporary relief of itching associated with minor skin irritations and rashes due to:
Warnings
For external use only
Do not use
When using this product
Stop use and ask a doctor if
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
for itching of skin irritation, inflammation, and rashes:
for external anal and genital itching, adults:
Other information
PRINCIPAL DISPLAY PANEL
BUDPAK ANTI-ITCH CREAM
Hydrocortisone 1%
NET WT 0.5 OZ. (14 g)
Inactive Ingredients
Purified Water, Mineral Oil, Propylene Glycol, Cetearyl Alcohol, Petrolatum, Glyceryl Stearate, Polysorbate 60, Sorbitan Stearate, Methylparaben, Propylparaben, Disodium Edta
* Please review the disclaimer below.