Benefit BOO BOO ZAP Medicated Acne Treatment

Benefit BOO BOO ZAP Medicated Acne Treatment by

Drug Labeling and Warnings

Benefit BOO BOO ZAP Medicated Acne Treatment by is a Otc medication manufactured, distributed, or labeled by Benefit Cosmetics, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BENEFIT BOO BOO ZAP MEDICATED ACNE TREATMENT- salicylic acid gel 
Benefit Cosmetics, 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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Benefit BOO BOO ZAP Medicated Acne Treatment

Drug Facts

Active Ingredient

Salicylic Acid 0.5%

Purpose

Acne treatment

Use

• for the treatment of acne
  

Warnings

For external use only. Avoid eye area.

When using this product using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug 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

Cleanse the skin thoroughly before applying. Cover the affected area with a thin layer 1 to 3 times a day. Because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Inactive ingredients

water (aqua), alcohol, sodium citrate, ppg-26-buteth-26, glycolic acid, peg-40 hydrogenated castor oil, bisabolol.

Boo boo zap! reduces, clears & helps prevent blemishes from occurring.

Dist. BENEFIT San Francisco CA 94104 USA
London W1H 5AF UK
Made in France benefitcosmetics.com

Benefit BOO BOO ZAP Medicated Acne Treatment 7.4ml (66472-034-01)

BENEFIT BOO BOO ZAP MEDICATED ACNE TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66472-034
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
GLYCOLIC ACID (UNII: 0WT12SX38S)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
LEVOMENOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66472-034-01	1 in 1 CARTON	12/29/2011	10/31/2017
1		7.4 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	12/29/2011	10/31/2017

Labeler - Benefit Cosmetics, LLC (070826813)

Registrant - Benefit Cosmetics, LLC (070826813)

Revised: 1/2020

Document Id: 9d211c7e-c17c-2193-e053-2995a90a1eeb

34390-5

Set id: 636a5752-7d86-431a-9864-194765bf2d7c

Version: 5

Effective Time: 20200127