ACNE CONTROL BODY WASH- salicylic acid wash soap

Acne Control Body Wash by

Drug Labeling and Warnings

Acne Control Body Wash by is a Otc medication manufactured, distributed, or labeled by RENU LABORATORIES INC., RENU LABORATORIES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Salicylic Acid

Two percent

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, contact physician or poison control center immediately.

Purpose

Acne Treatment

QUESTIONS

Call 844 425 4948

Made in the USA

Distributed by Clixit, LLC Orlando, FL

WARNINGS

Warnings

For external use only Using other topical acne medications at the same time may increase dryness or irritation of the skin

If bothersome dryness or irritation occurs use only one medication unless directed by doctor

Use:

For the treatment of acne.

DOSAGE & ADMINISTRATION

Directions

Use daily in shower or bath

For maximum lather massage over wet skin with a washcloth sponge or body puff concentrating on areas of the body prone to breakout

Rinse well

Other Ingredients:

Acrylates Copolymer, Aloe Barbadensis, Cannabis Sativa (Hemp) Seed Oil, Capryl Glycol, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Cocamidopropyl Betaine, Deionized Water, Ethylhexylglycerin, Glycerin, Glycolic Acid, Hexylene Glycol, Phenoxyethanol, Sodium C14-16 Olefin Sulfonate, Sodium Hydroxide, Tocopherol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNE CONTROL BODY WASH 
salicylic acid wash soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-441
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3.4 g  in 168 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCOLIC ACID (UNII: 0WT12SX38S)
TOCOPHEROL (UNII: R0ZB2556P8)
ALOE (UNII: V5VD430YW9)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CHAMOMILE (UNII: FGL3685T2X)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CITRIC ACID ACETATE (UNII: DSO12WL7AU)
ACRYLIC ACID/ISOPHORONE DIISOCYANATE/PEG-27 COPOLYMER (UNII: R0R8I3X29J)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-441-02	1 in 1 BOX	09/12/2019
1	NDC: 76348-441-01	168 g in 1 TUBE; 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	09/12/2019

Labeler - RENU LABORATORIES INC. (945739449)

Establishment
Name	Address	ID/FEI	Business Operations
RENU LABORATORIES INC		945739449	manufacture(76348-441)