ACNEFREE DERMATOLOGY INSPIRED CARE BLACKHEAD REMOVING SCRUB ACNE TREATMENT- salicylic acid gel

AcneFree Dermatology Inspired Care Blackhead Removing Scrub Acne Treatment by

Drug Labeling and Warnings

AcneFree Dermatology Inspired Care Blackhead Removing Scrub Acne Treatment by is a Otc medication manufactured, distributed, or labeled by Relumins Labs LLC, COSMESTHETIC LABS. CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2%

Uses

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

Inactive ingredients

cocus nucifera (coconut) oil, purified water, sodium hydroxide, glycine soja, aloe barbadensis leaf extract, olive oil, citrus sinesis oil, glycerin, sodium lactate, sodium glucconate, fragrance, CI 77492, CI 77891, kaolin clay and disodium EDTA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNEFREE DERMATOLOGY INSPIRED CARE BLACKHEAD REMOVING SCRUB ACNE TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79061-259
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCONUT OIL (UNII: Q9L0O73W7L)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SOYBEAN (UNII: L7HT8F1ZOD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
OLIVE OIL (UNII: 6UYK2W1W1E)
CITRUS SINENSIS FLOWER OIL (UNII: AJ56JP5TFP)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM GLUCONATE (UNII: R6Q3791S76)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
KAOLIN (UNII: 24H4NWX5CO)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79061-259-01	50 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 final	part333D	07/31/2018

Labeler - Relumins Labs LLC (081506626)

Establishment
Name	Address	ID/FEI	Business Operations
COSMESTHETIC LABS. CORP.		725862577	MANUFACTURE(79061-259)