SCAR- allantoin 0.5% gel

Scar by

Drug Labeling and Warnings

Scar by is a Otc medication manufactured, distributed, or labeled by Walgreens, Product Quest Mdf. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                   Purpose

Allantoin 0.5%........................Skin Protectant

PURPOSE

INDICATIONS & USAGE

Uses temporarily protects and helps relieve chapped or cracked skin

WarningsFor external use only

WHEN USING

When using this product do not get into eyes

STOP USE

Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days

DO NOT USE

Do not use on deep puncture wounds animal bites serious burns

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION

Directions Apply as needed

INACTIVE INGREDIENT

Inactive ingredients
Water, Glycerin, Glyceryl Acrylate/Acrylic Acid
Copolymer, Propylene Glycol, Allium Cepa
(Onion) Root Extract, Polysorbate 20, Sorbitol,
Lecithin, Xanthan Gum, Oleic Acid,
Beta-Glucan, Sodium Carbomer, Aloe
Barbadensis Leaf Extract, Juglans Regia
(Walnut) Seed Extract, Chamomilla Recutita
(Matricaria) Flower Extract, Fragrance,
Caprylyl Glycol, 1,2-Hexanediol,
Ethylhexylglycerin, Phenoxyethanol, Disodium
EDTA, Phytonadione.

OTHER SAFETY INFORMATION

Other information Store at room temperature

QUESTIONS

Questions? 1-888-287-1915

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SCAR 
allantoin 0.5% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-3131
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	Allantoin	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ONION (UNII: 492225Q21H)
Polysorbate 20 (UNII: 7T1F30V5YH)
Sorbitol (UNII: 506T60A25R)
Xanthan Gum (UNII: TTV12P4NEE)
Oleic Acid (UNII: 2UMI9U37CP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ENGLISH WALNUT (UNII: 1V3SHR7QB7)
CHAMOMILE (UNII: FGL3685T2X)
Caprylyl Glycol (UNII: 00YIU5438U)
1,2-Hexanediol (UNII: TR046Y3K1G)
Ethylhexylglycerin (UNII: 147D247K3P)
Phenoxyethanol (UNII: HIE492ZZ3T)
Phytonadione (UNII: A034SE7857)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-3131-01	1 in 1 CARTON	03/14/2017
1		20 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/14/2017

Labeler - Walgreens (008965063)

Registrant - Product Quest Mdf (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mdf		927768135	manufacture(0363-3131) , label(0363-3131)