nioxin PRO CLINICAL SCALP RECOVERY moisturizing conditioner by Wella Operations US LLC

nioxin PRO CLINICAL SCALP RECOVERY moisturizing conditioner by

Drug Labeling and Warnings

nioxin PRO CLINICAL SCALP RECOVERY moisturizing conditioner by is a Otc medication manufactured, distributed, or labeled by Wella Operations US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NIOXIN PRO CLINICAL SCALP RECOVERY MOISTURIZING CONDITIONER- pyrithione zinc lotion 
Wella Operations US LLC

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Drug Facts

Active Ingredient

Pyrithione zinc 0.5%

Purpose

Anti-dandruff

Uses

  • Helps prevent recurrence of flaking and itching associated with dandruff

Warnings

For external use only.

When using this product

  • Avoid contact with eyes. if contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

  • Condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • For best results use at least twice a week or as directed by a doctor.
  • Apply to wet scalp and hair, leave for 1-3 minutes. Rinse well.

Inactive ingredients water, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, dimethicone, glutamic acid, benzyl alcohol, phenoxyethanol, fragrance, methylparaben, mentha arvensis leaf oil, mentha piperita (peppermint) oil, citric acid, propylene glycol, linalool, hexyl cinnamal, camellia sinensis leaf extract, limonene, sodium polynaphthalenesulfonate, geraniol, DMDM hydantoin, cellulose gum, yeast extract, niacinamide, panthenol, biotin, lecithin, tocopheryl acetate, ethoxydiglycol, maltodextrin, glucose, propylparaben, lactic acid, sodium benzoate, equisetum arvense extract, rosmarinus officinalis (rosemary) leaf extract, salvia officinalis (sage) leaf extract, urtica dioica (nettle) extract, achillea millefolium extract, betula alba leaf extract, potassium sorbate, inositol, calcium pantothenate, tartaric acid, caramel.

Questions?

1-800-935-5273

NIOXIN SCALP RECOVERY™

MOISTURIZING CONDITIONER

HELPS TO REDUCE DANDRUFF AND PROVIDE SMOOTHNESS. AS PART OF A COMPLETE SCALP AND HAIR CARE SYSTEM, THIS CONDITIONER LEAVES HAIR NOURISHED, MOISTURIZED AND PROVIDES RESILIENCE AGAINST BREAKAGE.

MADE IN USA WITH IMPORTED PARTS

Dist. Wella Operations US LLC, Calabasas, CA 91302

www.nioxin.com

nioxin®

PRO CLINICAL

SCALP RECOVERY™

moisturizing conditioner

FOR ANTI-DANDRUFF

FOR ITCHY, FLAKY SCALP

COMBATS DANDRUFF FROM THE 1 ST USE

WITH PYRITHIONE ZINC

CLINICALLY & DERMATOLOGICALLY TESTED

200 mL (6.7 FL OZ)

82157-008-10_F82157-008-20_F82157-008-10_B82157-008-20_B

NIOXIN PRO CLINICAL SCALP RECOVERY MOISTURIZING CONDITIONER 
pyrithione zinc lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 82157-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
DIMETHICONE (UNII: 92RU3N3Y1O)  
MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH)  
NIACINAMIDE (UNII: 25X51I8RD4)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
GLUTAMIC ACID (UNII: 3KX376GY7L)  
CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PANTHENOL (UNII: WV9CM0O67Z)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SAGE (UNII: 065C5D077J)  
CARAMEL (UNII: T9D99G2B1R)  
STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
ROSEMARY (UNII: IJ67X351P9)  
LACTIC ACID (UNII: 33X04XA5AT)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
GERANIOL (UNII: L837108USY)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
BIOTIN (UNII: 6SO6U10H04)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
ETHOXYDIGLYCOL (UNII: A1A1I8X02B)  
INOSITOL (UNII: 4L6452S749)  
WATER (UNII: 059QF0KO0R)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
CITRIC ACID (UNII: 2968PHW8QP)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)  
YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)  
LIMONENE, (+/-)- (UNII: 9MC3I34447)  
BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO)  
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)  
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
FORMALDEHYDE/SODIUM NAPHTHALENESULFONATE COPOLYMER (3000 MW) (UNII: 90D834OZUI)  
CELLULOSE GUM (UNII: K679OBS311)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
GLUCOSE (UNII: 5SL0G7R0OK)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)  
URTICA DIOICA LEAF (UNII: X6M0DRN46Q)  
TARTARIC ACID (UNII: W4888I119H)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 82157-008-20200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/19/202412/31/2025
2NDC: 82157-008-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/19/202412/31/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03212/19/202412/31/2025
Labeler - Wella Operations US LLC (117781338)

Revised: 11/2025