DR THROWERS OILY SKIN FACIAL CLEANSER- salicylic acid 2% liquid

Dr Throwers Oily Skin Facial Cleanser by

Drug Labeling and Warnings

Dr Throwers Oily Skin Facial Cleanser by is a Otc medication manufactured, distributed, or labeled by Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 2%

Purpose

Acne treatment.

Uses

For the treatment of acne.

Warnings

For external use only.

When using this product skin irritation and dryness are 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.

Stop use if dryness, redness, or itching occurs and see a physician if symptoms persist.

Keep Out of Reach of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Use morning and evening. Apply to wet skin with fingers, massage lightly to foam. Avoid eye area, corners of the nose are, and around the mouth. Rinse thoroughly with warm water. If bothersome dryness or peeling occurs, reduce application to once a day or every other day or discontinue the product.

Inactive Ingredients

Ammonium laureth sulfate, ammonium lauryl sulfate, camphor, cocamide MEA, cocamidopropyl betaine, diazolidinyl urea, eucalyptus globulus leaf oil, glycol stearate, mentha piperita (peppermint) oil, menthol, methylparaben, PEG-150 pentaerythrityl tetrastearate, PEG-6 caprylic/capric glycerides, propylene glycol, propylparaben, sodium hydroxide, sodium laureth sulfate, water.

Label

INGREDIENTS AND APPEARANCE

DR THROWERS OILY SKIN FACIAL CLEANSER 
salicylic acid 2% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72839-613
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 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)
GLYCOL STEARATE (UNII: 0324G66D0E)
PEPPERMINT OIL (UNII: AV092KU4JH)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EUCALYPTUS OIL (UNII: 2R04ONI662)
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)
MENTHOL (UNII: L7T10EIP3A)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72839-613-02	57 g in 1 TUBE; Type 0: Not a Combination Product	09/28/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/28/2021

Labeler - Derma Care Research Labs, LLC (116817470)