Label: PANROSA FRESH CLEAN PYRITHIONE ZINC DANDRUFF- pyrithione zinc shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 50302-400-43 - Packager: Panrosa Enterprises, 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 October 20, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
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Inactive ingredients
Water, Sodium Larueth Sulfate, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Cocamide MEA, Glycol Distearate, Dimethicone, Trideceth-5, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Panthenol, Hydroxypropyl Guar, Cetearyl Alcohol, Fragrance, Allantoin, Disodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone.
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Panrosa FRESH CLEAN Pyrithione Zinc Dandruff Shampoo 443.66ml (50320-400-43)
PANROSA
FRESH CLEAN
BASIC HAIR CARE
Pyrithione Zinc Dandruff Shampoo
Deep cleaning for soothing relief of itchy, flaky scalp
15 fl oz (443.6 mL)
Distributed by:
Panrosa
ENTERPRISES, INC.
1969 S. Campus Ave.
Ontario, California 91761 U.S.A.
Made in China
Questions please visit our web site at www.panrosa.com
Package is recyclable where facilities exist.
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INGREDIENTS AND APPEARANCE
PANROSA FRESH CLEAN PYRITHIONE ZINC DANDRUFF
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50302-400 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCOL DISTEARATE (UNII: 13W7MDN21W) DIMETHICONE (UNII: 92RU3N3Y1O) TRIDECETH-5 (UNII: 76X6L6EU5K) SODIUM CHLORIDE (UNII: 451W47IQ8X) PANTHENOL (UNII: WV9CM0O67Z) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ALLANTOIN (UNII: 344S277G0Z) EDETATE DISODIUM (UNII: 7FLD91C86K) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50302-400-43 443.6 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package 03/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 03/01/2013 Labeler - Panrosa Enterprises, Inc. (859957578)