Otc - Active Ingredient
Active Ingredients
Allantoin 1% Skin Protectant
Scar Cream
FDA Label NDC 72982-1905
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Everyday Medical Llc for the product Scar Cream (NDC 72982-1905). 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 - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Skin protectant
Indications & Usage
temporarily protects and helps relieve chapped or cracked skin
Warnings
Warnings
For external use only
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 within a few days
Do not use on deep or punctured wounds, animal bites, serious burns
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away
Dosage & Administration
Apply as needed
Inactive Ingredient
CENTELLA ASIATICA
CYCLOMETHICONE 5
PHENYL TRIMETHICONE
ALKYL (C12-15) BENZOATE
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
WATER
CLOVE OIL
ALOE VERA LEAF
CETYL ALCOHOL
ONION
GLYCERIN
STEARIC ACID
EDETIC ACID
GLYCERYL STEARATE/PEG-100 STEARATE
MELALEUCA ALTERNIFOLIA LEAF
BUTYLATED HYDROXYTOLUENE
SODIUM HYDROXIDE
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE
PHYLLANTHUS EMBLICA WHOLE
TAMARIND
CETOSTEARYL ALCOHOL
CETEARYL GLUCOSIDE
* Please review the disclaimer below.
