CLEARSKIN BLACKHEAD ELIMINATING DAILY ASTRINGENT- salicylic acid liquid 
New Avon LLC

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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Active ingredient     

Salicylic Acid 2.0%.......................

                        Purpose
........................Acne Treatment

Uses

​Warnings

​For external use only.

​When using this product

  • ​avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, use only one topical acne medication at a time unless directed by a health care practitioner.

​Stop use and ask a health care practitioner if​ rash or irritation develops or increases.

​Keep out of reach of children

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

Flammable. Keep away from heat or flame. Keep out of direct sunlight.

Directions

DO NOT USE IF SEAL IS BROKEN.

Inactive ingredients SD alcohol 40-B, water/eau, propylene glycol, PEG-6, potassium hydroxide, benzophenone-1, parfum/fragrance, BHT, disodium EDTA, lysine carboxymethyl cysteinate, isododecane, aloe barbadensis leaf juice, sodium C8-16 isoalkylsuccinyl lactoglobulin sulfonate, polystyrene/
hydrogenated polyisopentene copolymer, chamomilla recutita (matricaria) flower extract, blue 1/CI 42090, red 33/CI 17200.

Questions? Call 1-800-FOR-AVON or 1-800-265-AVON in Canada.

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CLEARSKIN BLACKHEAD ELIMINATING  DAILY ASTRINGENT
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10096-0320
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
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10096-0320-1250 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/17/2014
Labeler - New Avon LLC (080143520)
Establishment
NameAddressID/FEIBusiness Operations
Avon Products, Inc.005149471manufacture(10096-0320)

Revised: 2/2016
Document Id: 1208738f-722f-420f-a324-8a819546715b
Set id: 5ad5f4b3-70c2-419a-bb41-ca092b20ac62
Version: 2
Effective Time: 20160219
 
New Avon LLC