GLY-SAL 10-2 PADS- salicylic acid cloth 
Topiderm, Inc.

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Gly-Sal® 10-2 Pads

Drug Facts

Active ingredient

Salicylic Acid USP, 2%

Purpose

Acne medication

Uses

Cleansing pads for the treatment of acne, with the skin enhancement properties of Glycolic acid.

Warnings

  • If irritation develops, discontinue use and consult a doctor.

  • Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

  • Keep out of reach of children. If swallowed, seek professional assistance or contact a Poison Control Center immediately.

  • Flammable; keep tightly closed, away from flame and heat.
  • Sunscreen use is recommended with any Glycolic Acid product and for an additional week thereafter, because some individuals may be more sensitive to sunlight.

Directions

Inactive ingredients

Purified Water, Glycolic Acid, SD Alcohol 40B(13% v/v), Hamamelis Virginiana (Witch Hazel) Water, Ammonium Hydroxide, Polysorbate-20, Sodium Benzoate, Imidazolidinyl Urea, Acetone, Disodium EDTA.

PRINCIPAL DISPLAY PANEL - 60 Pad Jar Label

REPLENiX®
ACNE SOLUTIONS

Topix Pharmaceuticals, Inc.
N. Amityville, NY 11701

Gly/Sal® 10-2
Pads

Glycolic Acid 10%
Salicylic Acid USP, 2%

60 Pads

PRINCIPAL DISPLAY PANEL - 60 Pad Jar Label
GLY-SAL 10-2 PADS 
salicylic acid cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51326-039
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.02 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
ALCOHOL (UNII: 3K9958V90M)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
AMMONIA (UNII: 5138Q19F1X)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
IMIDUREA (UNII: M629807ATL)  
ACETONE (UNII: 1364PS73AF)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51326-039-6060 in 1 JAR; Type 0: Not a Combination Product07/28/2000
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM00607/28/2000
Labeler - Topiderm, Inc. (049121643)
Registrant - Topiderm, Inc. (049121643)
Establishment
NameAddressID/FEIBusiness Operations
Topiderm, Inc.049121643MANUFACTURE(51326-039)
Establishment
NameAddressID/FEIBusiness Operations
Topix Pharmaceuticals, Inc.117745066PACK(51326-039)

Revised: 10/2019
Document Id: 39700b88-6308-4682-b1b2-107140d92913
Set id: b39e845d-4c40-4f9e-9cb5-a8386f326652
Version: 4
Effective Time: 20191023
 
Topiderm, Inc.