Label: PERFECT PURITY OIL FREE ACNE WASH- salicyclic acid rinse
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Contains inactivated NDC Code(s)
NDC Code(s): 71319-009-06 - Packager: 9338-9641 Quebec Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 13, 2017
If you are a consumer or patient please visit this version.
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- Active Ingredient
- Purpose
- Use
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Warnings
For external use only.
Ask a doctor or pharmacist before use if
you are using other topical acne medication at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used, unless directed by a doctor.
- Directions
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INACTIVE INGREDIENT
Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, PEG-150 Distearate, Propylene Glycol, Cocamide MEA, PEG-80 Sorbitan Laurate, Dipropylene Glycol, Sodium Chloride, Fragrance, Methylisothiazolinone, Methylchloroisothiazolinone, Aloe Barbadensis Leaf Extract, Anthemis Nobilis Flower Extract, Disodium EDTA, Yellow 5 (19140), Red 40 (Cl 1605)
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INGREDIENTS AND APPEARANCE
PERFECT PURITY OIL FREE ACNE WASH
salicyclic acid rinseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71319-009 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 WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) COCO MONOETHANOLAMIDE (UNII: C80684146D) PEG-80 SORBITAN LAURATE (UNII: 239B50Y732) DIPROPYLENE GLYCOL (UNII: E107L85C40) SODIUM CHLORIDE (UNII: 451W47IQ8X) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71319-009-06 177 g in 1 BOTTLE; Type 0: Not a Combination Product 03/13/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 03/13/2017 Labeler - 9338-9641 Quebec Inc (203329870) Registrant - 9338-9641 Quebec Inc (203329870)