REFINE COMPLEXION CLEARING PADS- salicylic acid swab

REFINE by

Drug Labeling and Warnings

REFINE by is a Otc medication manufactured, distributed, or labeled by SCHWEIGER DERMATOLOGY GROUP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Salicylic Acid 2.00%

Purpose

Acne Treatment

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
• When using this product, rinse immediately with water if it gets in eyes.
• If swallowed, consult a physician or poison control center.

Directions

• Clean the skin thoroughly before applying this product.
• 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 the application to once a day or every other day.
• If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Additional Information

Store at room temperature.

Inactive ingredients

Purified Water, SD Alcohol 40B, Propylene Glycol, Salicylic Acid, Glycolic Acid, Mandelic Acid, Polysorbate 20, Calendula Extract, Butylene Glycol, Cucumber Extract, Chamomile Extract, Aloe Baradensis Leaf Extract, Ammonium Hydroxide, Phenoxyethanol, Ethylhexyglycerin.

Questions

1 888 311 7444

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Distributed by: Schweiger Dermatology Group
NY, NY 10019

PRINCIPAL DISPLAY PANEL - 60 Pad Carton

SKIN SOLUTIONS
dr.Schweiger
NEW YORK

Refine
Complexion Clearing Pads

2% Glycolic + 2% Salicylic Pads

60 pads

INGREDIENTS AND APPEARANCE

REFINE   COMPLEXION CLEARING PADS
salicylic acid swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70911-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
salicylic acid (UNII: O414PZ4LPZ) (salicylic acid - UNII:O414PZ4LPZ)	salicylic acid	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCOLIC ACID (UNII: 0WT12SX38S)
MANDELIC ACID (UNII: NH496X0UJX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
calendula officinalis flowering top (UNII: 18E7415PXQ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CHAMOMILE (UNII: FGL3685T2X)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMMONIA (UNII: 5138Q19F1X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Product Characteristics
Color	WHITE	Score
Shape	ROUND	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70911-110-12	1 in 1 CARTON	01/01/2017
1	NDC: 70911-110-11	60 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	01/01/2017

Labeler - SCHWEIGER DERMATOLOGY GROUP (007492566)