NEUTRALYZE SPOT TREATMENT- salicylic acid gel

NEUTRALYZE SPOT TREATMENT by

Drug Labeling and Warnings

NEUTRALYZE SPOT TREATMENT by is a Otc medication manufactured, distributed, or labeled by KANTIAN SKINCARE, LLC, PhytogenX. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient:

Salicylic acid 1.0%

PURPOSE

Uses:

Treats and helps prevent acne blemishes.

Warnings:

For external use only. Avoid contact with eyes. If contact occurs, flush thoroughly with water. Using other topical acne medications at the same time or right after use of this product may increase skin dryness or irritation. Avoid doing this, unless directed by a doctor. Avoid unnecessary sun exposure and use sunscreen. Allow Neutralyze Spot Treatment to dry, then follow the sunscreen directions. Do not use this product if you have sensitive skin or if you are sensitive to AHAs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. Do not use this product on infants under 6 months of age.

Directions:

Apply a thin layer to the affected area, in the morning and evening. For best results, apply Neutralyze Synergyzer after Neutralyze Spot Treatment.

Inactive ingredients:

Water, Isopropyl alcohol, Propylene glycol, Hydroxyethylcellulose, Mandelic acid, Poloxamer P103, Sodium benzoate, FD&C Blue #1

Distributed by: Kantian Skincare, LLC. Smithtown, NY, 11787. Made in USA © 2012.

Principal Display Panel - 28g Bottle Label

neutralyze

SPOT TREATMENT

ANTI-ACNE SOLUTION

Eliminates Acne Causing Bacteria

Clears Acne Pimples and Blackheads Quickly

Gentle Enough for Everyday Use

Dermatologist Recommended

MADE IN USA

NET WT. 1 OZ (28g)

INGREDIENTS AND APPEARANCE

NEUTRALYZE SPOT TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57524-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	1.0 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isopropyl Alcohol (UNII: ND2M416302)
Propylene Glycol (UNII: 6DC9Q167V3)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
Mandelic Acid (UNII: NH496X0UJX)
Sodium Benzoate (UNII: OJ245FE5EU)
FD&C Blue No. 1 (UNII: H3R47K3TBD)
Propylene Oxide (UNII: Y4Y7NYD4BK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57524-014-01	28 g in 1 BOTTLE; Type 0: Not a Combination Product	11/03/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	11/03/2014

Labeler - KANTIAN SKINCARE, LLC (078436984)

Establishment
Name	Address	ID/FEI	Business Operations
PhytogenX		624386772	MANUFACTURE(57524-014)