Label: HEAD AND SHOULDERSVOLUME BOOST HAIR AND SCALP CONDITIONER- pyrithione zinc lotion
- NDC Code(s): 69423-151-31, 69423-151-38, 69423-151-40
- 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 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- Questions (or comments)?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 315 mL Tube Label
-
INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERSVOLUME BOOST HAIR AND SCALP CONDITIONER
pyrithione zinc lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-151 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 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) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) WATER (UNII: 059QF0KO0R) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-151-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/2016 06/15/2019 2 NDC:69423-151-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/11/2017 09/24/2020 3 NDC:69423-151-31 315 mL in 1 TUBE; Type 0: Not a Combination Product 11/29/2018 12/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M032 11/21/2016 12/01/2024 Labeler - The Procter & Gamble Manufacturing Company (004238200)