Active Ingredient
White petrolatum USP (30%)
Lucky Super Soft
FDA Label NDC 47046-171
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anicare Pharmaceuticals Pvt. Ltd. for the product Lucky Super Soft (NDC 47046-171). 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, when using this product, stop use and ask a doctor if, do not use on, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin protectant
Uses
■ temporarily protects minor ■ cuts ■ scrapes ■ burns ■ temporarily protects and helps relieve chapped or cracked skin ■ helps prevent and protect from the drying effects of wind and cold weather
Warnings
For External Use Only
When Using This Product
do not get into eyes
Stop Use And Ask A Doctor If
■ condition worsens ■ symptoms last more than 7 days or clear up and occur again in a few days
Do Not Use On
■ deep or puncture wounds ■ animal bites ■ serious burns
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
apply as needed
Inactive Ingredients
water, cetearyl alcohol, ceteareth 20, glycerin, mineral oil, fragrance, benzyl alcohol, methylchloroisothaizolinone, methylisothaizolinone, titanium dioxide, citric acid, tocopheryl acetate
Package Label
Package Label (Petjlycrmwvite)
* Please review the disclaimer below.
