DHC SALICYLIC ACNE WASH- salicylic acid lotion 
DHC USA Incorporated

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.

----------

DHC Salicylic Acne Wash

Drug Facts

Active Ingredients

Salicylic acid 2%

Purpose

Acne treatment

Uses

Warnings

For external use only.

  • Using other topical acne medications at the same time or immediately following the 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, get medical help or contact a Poison Control Center right away.

Directions

Wet face with lukewarm water. Create lather in palms, then massage face with foam to cleanse. Rinse thoroughly. For best results, use with DHC Acne Spot Therapy.

Inactive Ingredients

water, ammonium laureth sulfate, cetyl alcohol, cocamidopropyl betaine, glycol distearate, cocamide MEA, triethanolamine, phenoxyethanol, polyethylene, steareth-20, guar hydroxypropyltrimonium chloride, disodium EDTA, rosmarinus officinalis (rosemary) leaf oil, butylene glycol, allantoin, camellia sinensisleaf extract, royal jelly extract, scutellaria baicalensis root extract, houttuynia cordata extract, perilla ocymoides leaf extract, aloe barbadensis leaf extract

Questions or Comments?

1-800-DHC-CARE (342-2273)

www.DHCcare.com

Distributed by DHC USA Inc.
Mechanicsburg, PA 17050

PRINCIPAL DISPLAY PANEL - 120 ml Bottle Carton

DHC

Salicylic
Acne Wash

Acne treatment
4 fl. oz. U.S. (120 ml)

PRINCIPAL DISPLAY PANEL - 120 ml Bottle Carton
DHC SALICYLIC ACNE WASH 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63433-383
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid30 mg  in 1.5 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Ammonium Lauryl Sulfate (UNII: Q7AO2R1M0B)  
Cetyl Alcohol (UNII: 936JST6JCN)  
Glycol Distearate (UNII: 13W7MDN21W)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
Coco Monoethanolamide (UNII: C80684146D)  
Trolamine (UNII: 9O3K93S3TK)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Steareth-20 (UNII: L0Q8IK9E08)  
Guar Hydroxypropyltrimonium Chloride (1.7 Substituents per Saccharide) (UNII: B16G315W7A)  
Edetate Disodium (UNII: 7FLD91C86K)  
Rosemary Oil (UNII: 8LGU7VM393)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Allantoin (UNII: 344S277G0Z)  
Green Tea Leaf (UNII: W2ZU1RY8B0)  
Royal Jelly (UNII: L497I37F0C)  
Scutellaria Lateriflora Top (UNII: C6CNB75R61)  
Houttuynia Cordata Flowering Top (UNII: RH041UUZ22)  
Perilla Frutescens Leaf (UNII: T4L5881Y68)  
Aloe Vera Leaf (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63433-383-001 in 1 CARTON11/01/2018
1120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D11/01/2018
Labeler - DHC USA Incorporated (004087554)
Registrant - ABBE Laboratories, Inc. (781745286)
Establishment
NameAddressID/FEIBusiness Operations
ABBE Laboratories, Inc.781745286MANUFACTURE(63433-383)

Revised: 2/2022
Document Id: da98f1be-9181-47c7-8066-dd1e48e27e3d
Set id: b7020e5b-4b51-4fc5-abe9-070593a73ff8
Version: 2
Effective Time: 20220228
 
DHC USA Incorporated