SKIN CLEARIFY SPOT TREATMENT- salicylic acid liquid 
Herbalife International of America Inc.

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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Clearify Acne Spot Treatment

Drug Facts

Active ingredient

Salicylic acid (1.5%)

Purpose

Acne treatment

Uses

For the treatment of acne. Dries up 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

Inactive ingredients: Water (Aqua), Butylene Glycol, Aloe Barbadensis Leaf Juice, SD Alcohol 40-B, Silica, Niacinamide, Polyacrylate Crosspolymer-6, Hamamelis Virginiana (Witch Hazel) Water, Castanea Sativa (Chestnut) Seed Extract, Physalis Angulata Extract, Caprylic/Capric Triglyceride, Xanthan Gum, Disodium EDTA, Triethanolamine, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol.

Distributed by: Herbalife International of America, Inc.

800 W. Olympic Blvd., Suite 406, Los Angeles, CA 90015 USA

Made in USA with US and imported ingredients.

© 2016 HERBALIFE

HERBALIFE

SKIN Clearify

Spot Treatment

Salicylic Acid Acne Treatment

0.5 fl oz (15 mL)

01_Spot Treatment

SKIN CLEARIFY SPOT TREATMENT 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51785-809
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1.5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
NIACINAMIDE (UNII: 25X51I8RD4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALCOHOL (UNII: 3K9958V90M)  
PHYSALIS ANGULATA (UNII: W4TKW9D5GG)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
CASTANEA SATIVA WHOLE (UNII: DK55N3C1AK)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
TROLAMINE (UNII: 9O3K93S3TK)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51785-809-001 in 1 CARTON10/01/2016
115 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D10/01/2016
Labeler - Herbalife International of America Inc. (873035968)

Revised: 10/2016
Document Id: 3e88a845-afec-6ec5-e054-00144ff8d46c
Set id: 339c99b7-bf87-52c0-e054-00144ff8d46c
Version: 2
Effective Time: 20161010
 
Herbalife International of America Inc.