Label: HEAD AND SHOULDERS DRY SCALP CARE HAIR AND SCALP CONDITIONER- pyrithione zinc lotion
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NDC Code(s):
69423-160-32,
69423-160-40,
69423-160-59,
69423-160-65, view more69423-160-68
- Packager: The Procter & Gamble Manufacturing Company
- 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 2, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- Questions (or comments)?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 325 mL Tube Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS DRY SCALP CARE HAIR AND SCALP CONDITIONER
pyrithione zinc lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-160 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL ALCOHOL (UNII: 936JST6JCN) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) GLUTAMIC ACID (UNII: 3KX376GY7L) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZYL ALCOHOL (UNII: LKG8494WBH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALMOND OIL (UNII: 66YXD4DKO9) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-160-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/10/2016 12/10/2020 2 NDC:69423-160-68 680 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/10/2016 12/10/2020 3 NDC:69423-160-32 325 mL in 1 TUBE; Type 0: Not a Combination Product 11/29/2018 4 NDC:69423-160-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 11/01/2024 5 NDC:69423-160-59 592 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M032 11/10/2016 Labeler - The Procter & Gamble Manufacturing Company (004238200)