Active Ingredient(S)
Allantoin 0.3%
Scar Gel
FDA Label NDC 75728-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Meayon Biotechnology Co,.ltd for the product Scar Gel (NDC 75728-004). 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(s), purpose, use, warnings, 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.
Label Section Quick Index
Purpose
Skin Protectant
Use
Temporarily protects and helps relieve chapped or cracked skin.
Warnings
For external use only.
Do Not Use
/
Otc - When Using
do not get into eyes.
Otc - Stop Use
condition worsens symptoms last more than 7daysor clear up and occur again within a few days DO not use on.
deep or puncture wounds animal bites serious burns.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
condition worsens symptoms last more than 7daysor clear up and occur again within a few days DO not use on.
Other Information
/
Inactive Ingredients
CYCLOPENTASILOXANE
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER
HEXYLDECANOL
STEARIC ACID
BRASSICA CAMPESTRIS (RAPESEED) STEROLS
ARGANIA SPINOSA KERNEL OIL
TOCOPHERYL ACETATE
CERAMIDE 3
CERAMIDE 6 II
CHOLESTEROL
MADECASSOSIDE
Package Label - Principal Display Panel
75728-004-01 15 g in 1 BOTTLE
75728-004-02 20 g in 1 BOTTLE
75728-004-03 30 g in 1 BOTTLE
* Please review the disclaimer below.
