THAYERS SINCE 1847 NATURAL REMEDIES BLEMISH CLEARING WITCH HAZEL ALOE VERA FORMULA CLEANSER- salicylic acid gel 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient


Salicylic acid 2%

Purpose

Acne treatment

Uses

• for the treatment of acne
• clears acne blemishes and allows skin to heal
• helps prevent the development of new acne blemishes

Warnings

For external use only

When using this product

skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

store at 15°-30° C (59°-86° F) away from direct sunlight

Inactive ingredients

water, natural beatine, glycerin, lauryl glucoside, sodium cocoyl isethionate, decyl glucoside, hamamelis virginiana (witch hazel) bark/leaf/twig extract, aloe barbadensis leaf extract, phenoxyethanol, ethylhexylglycerin, cymbopogon schoenanthus (lemongrass) leaf extract blend, melaleuca
alternafolia (tea tree) leaf oil, hydroxypropyl methylcellulose, guar cydroxypropyltrimonium chloride

image of a label

image of a label
THAYERS SINCE 1847 NATURAL REMEDIES BLEMISH CLEARING WITCH HAZEL ALOE VERA FORMULA CLEANSER 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-051
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
TEA TREE OIL (UNII: VIF565UC2G)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-051-01118 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00601/01/2022
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
Continental Manufacturing Chemist081171390manufacture(49967-051)

Revised: 12/2023
Document Id: c01a122f-7b2e-4caa-9d8c-5d1c30970225
Set id: 935a58f0-d9a3-4423-9a5f-65fd19fad3db
Version: 2
Effective Time: 20231227
 
L'Oreal USA Products Inc