MEDICATED WASH- salicylic acid liquid

Medicated Wash by

Drug Labeling and Warnings

Medicated Wash by is a Otc medication manufactured, distributed, or labeled by Vivier Pharma, Inc., Dermolab Pharma Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid USP 2%

Purpose

Acne Treatment

Uses

For the treatment of acne. Dries, clears and helps keep skin clear of new acne pimples, blackheads and white heads.

WARNINGS For exrernal use only

Ask a doctor before use if you are

• Using other topical acne medications 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

When using this product

• Do not get into eyes.

Stop use and ask a doctor if

• Excessive skin irritation develops or increases.

Keep out of reach of children.

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

Directions

• ​Wet face using lukewarm water.
• Gently massage over the face using fingertips.
• Rinse completely.
• Use both morning and night or as directed by a physician.
• If dryness or peeling occurs, reduce application to once a day or every other day.

Other Information

• Store at room temperature
  
  (15-30°C / 59-86°F).

Inactive Ingredients

Acrylates Copolymer, Alcohol, Citric Acid, Disodium
Cocoamphodiacetate, Disodium Cocoyl Glutamate,
DMDM Hydantoin, Ethoxydiglycol, Fragrance,
Hexamidine Diisethionate, PEG-7 Glyceryl Cocoate,
PEG-120 Methyl Glucose Dioleate, Sodium
Hydroxide, Sodium Lauroyl Sarcosinate, Water / Eau.

Package Label

INGREDIENTS AND APPEARANCE

MEDICATED WASH 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67226-1021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
HEXAMIDINE DIISETHIONATE (UNII: 023XA5Z50L)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67226-1021-1	150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/11/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/11/2017

Labeler - Vivier Pharma, Inc. (250996550)

Establishment
Name	Address	ID/FEI	Business Operations
Dermolab Pharma Ltd		245414743	manufacture(67226-1021)