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Scar Equate

Dosage form: gel
Ingredients: ALLANTOIN 0.5g in 100g
Labeler: Walmart
NDC Code: 49035-951

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts FR#33-255PQ

Active ingredient                   Purpose

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

Uses temporarily protects and helps relieve chapped or cracked skin


Warnings
For external use only

When using this product • do not get into eyes

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 on • deep puncture wounds • animal bites • serious burns

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

Directions • Apply as needed

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 information Store at room temperature

SCAR   EQUATE
allantoin 0.5% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-951
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ONION 
POLYSORBATE 20 
SORBITOL 
XANTHAN GUM 
OLEIC ACID 
ALOE VERA LEAF 
ENGLISH WALNUT 
CHAMOMILE 
CAPRYLYL GLYCOL 
1,2-HEXANEDIOL 
ETHYLHEXYLGLYCERIN 
PHENOXYETHANOL 
EDETATE DISODIUM 
PHYTONADIONE 
WATER 
Packaging
#Item CodePackage Description
1NDC:49035-951-031.76 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34702/02/2015
Labeler - Walmart (051957769)
Registrant - Product Quest Mdf (927768135)
Establishment
NameAddressID/FEIOperations
Product Quest Mdf927768135manufacture(49035-951), label(49035-951)

Revised: 01/2018
 
Walmart

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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