ACNE FIGHTING PUTTY PRIMER- salicylic acid cream

Acne Fighting Putty Primer by

Drug Labeling and Warnings

Acne Fighting Putty Primer by is a Otc medication manufactured, distributed, or labeled by e.l.f. Cosmetics, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Salicylic Acid 1.8%

Purpose

Acne Treatment

Use

• For the treatment of acne
• Helps prevent new acne blemishes

Warnings

For external use only.

• Keep out of eyes. Rinse with water to remove.
• Skin irritation and dryness is more likely to occur if you use another topical acne medication at a time.

Stop use and ask a doctor if

rash occurs.

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 medication.
• Cover the entire affected area with a thin layer one to three times daily.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
• If bothersome dryness or peeling occurs, reduce application to once a day every other day.

Inactive Ingredients

Water (Aqua), Dimethicone, Propylene Glycol, Glycerin, Ceresin, Paraffin, Hydrogenated Polyisobutene, HDI/Trimethylol Hexyllactone Crosspolymer, Trimethylsiloxysilicate, Polymethylsilsesquioxane, Tromethamine, Tromethamine Sodium Chloride, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone Crosspolymer, Zinc PCA, Kaolin, Silica, Oryza Sativa (Rice) Bran Wax, Triethoxycaprylylsilane, Disodium EDTA, Ethylhexylglycerin, Caprylyl Glycol, Phenoxyethanol May contain: Titanium Dioxide (CI 77891), Chromium Oxide Greens (CI 77288), Yellow Iron Oxide (CI 77492)

Questions or comments?

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Packge Labeling:

INGREDIENTS AND APPEARANCE

ACNE FIGHTING PUTTY PRIMER 
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-412
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	18 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
CERESIN (UNII: Q1LS2UJO3A)
PARAFFIN (UNII: I9O0E3H2ZE)
HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
TROMETHAMINE (UNII: 023C2WHX2V)
DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)
ZINC PIDOLATE (UNII: C32PQ86DH4)
KAOLIN (UNII: 24H4NWX5CO)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
RICE BRAN (UNII: R60QEP13IC)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-412-21	1 in 1 BOX	02/20/2021
1		21 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	02/20/2021

Labeler - e.l.f. Cosmetics, Inc (093902816)