DERMACLEAR PADS- salicylic acid liquid 
Allure Labs

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.

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Drug Facts

Active Ingredient - Salicylic Acid 2%

Purpose: Acne Treatment

Uses: For treatment of Acne

Warnings:

Do not use if you have sensitive skin.

When using this product:

Stop use and ask a doctor:

Keep out of reach of children:

Gently rub pad over any area in need. Use every other night or as recommended by your skin care prifessional. Keep the lid securely closed to prevent evapration. To avoid dryness, do not overuse. Not recommended for those with aspirin / NASID allergies.

Inactive Ingredients:

Alcohol Denat., Water (Aqua), Glycerin, PEG-8/SMDI Copolymer, Glycolic Acid, Aloe Barbadensis Leaf Juice, Ammonium Hydroxide, Melaleuca Alternifolia Leaf Oil, Allantoin, Limonene.

Manufactured for DermaQuest®, Inc.

Hayward, CA 94544

1272 GK, NL Made in USA

dermaquestinc.com

IMGDERMPADS

DERMACLEAR PADS 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4076
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
AMMONIA (UNII: 5138Q19F1X)  
TEA TREE OIL (UNII: VIF565UC2G)  
ALLANTOIN (UNII: 344S277G0Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62742-4076-21 in 1 CARTON05/08/2015
1NDC:62742-4076-185 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D05/08/2015
Labeler - Allure Labs (926831603)
Registrant - Allure Labs (926831603)
Establishment
NameAddressID/FEIBusiness Operations
Allure Labs926831603manufacture(62742-4076)

Revised: 11/2020
Document Id: b55e159b-70d3-5f1e-e053-2a95a90afc5a
Set id: 0c6624fd-88f9-402c-8ac2-bc278242b484
Version: 2
Effective Time: 20201130
 
Allure Labs