ACNE FREE BLACKHEAD REMOVING SCRUB 2 SALICYLIC ACID WITH CHARCOAL- salicylic acid gel

Acne Free BLACKHEAD REMOVING SCRUB 2 Salicylic Acid with Charcoal by

Drug Labeling and Warnings

Acne Free BLACKHEAD REMOVING SCRUB 2 Salicylic Acid with Charcoal by is a Otc medication manufactured, distributed, or labeled by AcneFree LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Use

for the treatment of acne

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

wet hands and face
squeeze scrub into hands and rub together
apply to face and massage gently, avoiding contact with eyes. If contact occurs, rinse thoroughly with water.
rinse face

Inactive ingredients

water, sodium laureth sulfate, perlite, sodium chloride, acrylates copolymer, sodium hydroxide, coco-betaine, cocamide MEA, glycerin, citric acid, trisodium ethylenediamine disuccinate, hydrogenated castor oil, propylene glycol, hydrogenated jojoba oil, iron oxides, charcoal powder, sorbitol, vaccinium myrtillus fruit extract, polyglycerin-10, polyglyceryl-10 myristate, polyglyceryl-10 stearate, sodium dehydroacetate, PPG-5-ceteth-20

Questions or comments?

1-888-768-2913

Package Labeling:

INGREDIENTS AND APPEARANCE

ACNE FREE BLACKHEAD REMOVING SCRUB 2 SALICYLIC ACID WITH CHARCOAL 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80861-012
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
FERRIC OXIDE RED (UNII: 1K09F3G675)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
SORBITOL (UNII: 506T60A25R)
BILBERRY (UNII: 9P2U39H18W)
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
PERLITE (UNII: 0SG101ZGK9)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCO-BETAINE (UNII: 03DH2IZ3FY)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO)
POLYGLYCERIN-10 (UNII: P9060O936A)
POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80861-012-01	150 mL in 1 TUBE; Type 0: Not a Combination Product	07/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	07/31/2018

Labeler - AcneFree LLC (122237140)