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

Dr Throwers Oily Skin Facial Astringent by

Drug Labeling and Warnings

Dr Throwers Oily Skin Facial Astringent 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

Dries and clears acne blemishes and allows skin to heal.

Warnings

For external use only.

Flammable--Keep away from open fire or flame.

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.

Keep Out of Reach of Children.

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

Directions

• Clean the skin thoroughly before applying this product
• Using a cotton ball, cover the entire affected area with a thin layer one to three times daily
• Avoid eye area, corner of the nose, and around the mouth area
• 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 directed by a doctor
• If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive Ingredients

Alcohol denat., benzoic acid, blue 1, boric acid, butylene glycol, eucalyptus globulus leaf oil, lavandula angustifolia (lavender) oil, mentha piperita (peppermint) oil, menthol, polysorbate 20, red 33, water.

Label

INGREDIENTS AND APPEARANCE

DR THROWERS OILY SKIN FACIAL ASTRINGENT 
salicylic acid 2% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72839-611
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
BORIC ACID (UNII: R57ZHV85D4)
PEPPERMINT OIL (UNII: AV092KU4JH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
ALCOHOL (UNII: 3K9958V90M)
BENZOIC ACID (UNII: 8SKN0B0MIM)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
EUCALYPTUS OIL (UNII: 2R04ONI662)
LAVENDER OIL (UNII: ZBP1YXW0H8)
MENTHOL (UNII: L7T10EIP3A)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72839-611-02	57 g in 1 BOTTLE, PLASTIC; 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)