NIOXIN

Main information

  • Trade name:
  • NIOXIN SCALP RECOVERY SOOTHING SERUM pyrithione zinc liquid
  • Composition:
  • PYRITHIONE ZINC 0.97 mg in 1 mL
  • Prescription type:
  • OTC DRUG
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • NIOXIN SCALP RECOVERY SOOTHING SERUM pyrithione zinc liquid
    United States
  • Language:
  • English

Status

  • Source:
  • DailyMed - NLM - National Library of Medicine
  • Authorization status:
  • OTC monograph final
  • Last update:
  • 15-01-2018

Summary of Product characteristics: dosage, interactions, side effects

NIOXIN SCALP RECOVERY SOOTHING SERUM- pyrithione zinc liquid

The Procter & Gamble Manufacturing Company

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.

----------

Nioxin

Scalp Recovery

Soothing Serum

Drug Facts

Active ingredient

Pyrithione Zinc 0.1%

Purpos e

Anti-dandruff, Anti-seborrheic dermatitis

Us es

helps prevent recurrence of flaking, itching, irritation, scaling and redness associated with dandruff

and seborrheic dermatitis.

Warnings

For external use only.

Ask a doctor before use if you have a condition that covers a large area of the body.

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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison

Control Center right away.

Directions

apply to affected areas one to four times daily or as directed by a doctor.

Inactive ingredients

water, stearamidopropyl dimethylamine, cetyl alcohol, hydroxyethylcellulose, quaternium-18, benzyl

alcohol, phenoxyethanol, stearyl alcohol, PEG-2M, dimethicone, cetearyl alcohol, methylparaben,

propylparaben, fragrance, glyceryl stearate, oleyl alcohol, citric acid, polysorbate 60, mentha piperita

(peppermint) oil, menthol, mentha arvensis leaf oil, yeast extract, camellia sinensis leaf extract, lecithin,

PPG-26-buteth-26, saccharomyces/magnesium ferment, dimethyl isosorbide, carnitine HCL, PEG/PPG-

18/18 dimethicone, ethoxydiglycol, oryza sativa (rice) bran, PEG-40 hydrogenated castor oil,

biotin/folic acid/cyanocobalamin/niacinamide/pantothenic acid/pyridoxine/riboflavin/thiamine/yeast

polypeptides, saccharomyces/iron ferment, saccharomyces/copper ferment, saccharomyces/silicone

®

®

ferment, saccharomyces/zinc ferment, acacia senegal gum, ubiquinone.

Ques tions ?

1-800-935-5273

Dist. by THE WELLA

CORPORATION, WOODLAND

HILLS, CA 91367

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton

NIOXIN

SCALP RECOVERY

For a dry, itchy scalp

PYRITHIONE ZINC

DANDRUFF AND

SEBORRHEIC

DERMATITIS

TREATMENT

SOOTHING

SERUM

100% FLAKE FREE

ELIMINATION OF

VISIBLE FLAKES WITH

REGULAR USE*

100 mL (3.38 FL OZ)

®

®

NIOXIN SCALP RECOVERY SOOTHING SERUM

pyrithione zinc liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:370 0 0 -733

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

PYRITHIO NE ZINC (UNII: R9 53O2RHZ5) (PYRITHIONE ZINC - UNII:R9 53O2RHZ5)

PYRITHIONE ZINC

0 .9 7 mg in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

STEARAMIDO PRO PYL DIMETHYLAMINE (UNII: K7VEI0 0 UFR)

CETYL ALCO HO L (UNII: 9 36 JST6 JCN)

Q UATERNIUM-18 (UNII: O7757NO1VL)

BENZYL ALCO HO L (UNII: LKG8 49 4WBH)

PHENO XYETHANO L (UNII: HIE49 2ZZ3T)

STEARYL ALCO HO L (UNII: 2KR8 9 I4H1Y)

DIMETHICO NE (UNII: 9 2RU3N3Y1O)

CETO STEARYL ALCO HO L (UNII: 2DMT128 M1S)

METHYLPARABEN (UNII: A2I8 C7HI9 T)

PRO PYLPARABEN (UNII: Z8 IX2SC1OH)

GLYCERYL MO NO STEARATE (UNII: 230 OU9 XXE4)

O LEYL ALCO HO L (UNII: 172F2WN8 DV)

CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP)

PO LYSO RBATE 6 0 (UNII: CAL22UVI4M)

PEPPERMINT O IL (UNII: AV0 9 2KU4JH)

MENTHO L, UNSPECIFIED FO RM (UNII: L7T10 EIP3A)

MENTHA ARVENSIS LEAF O IL (UNII: 1AEY1M553N)

YEAST, UNSPECIFIED (UNII: 3NY3SM6 B8 U)

GREEN TEA LEAF (UNII: W2ZU1RY8 B0 )

DIMETHYL ISO SO RBIDE (UNII: SA6 A6 V432S)

CARNITINE CHLO RIDE (UNII: F6 426 4D6 3N)

PEG/PPG-18 /18 DIMETHICO NE (UNII: 9 H0 AO7T79 4)

DIETHYLENE GLYCO L MO NO ETHYL ETHER (UNII: A1A1I8 X0 2B)

RICE BRAN (UNII: R6 0 QEP13IC)

PO LYO XYL 4 0 HYDRO GENATED CASTO R O IL (UNII: 7YC6 8 6 GQ8 F)

BIO TIN (UNII: 6 SO6 U10 H0 4)

FO LIC ACID (UNII: 9 35E9 7BOY8 )

CYANO CO BALAMIN (UNII: P6 YC3EG20 4)

NIACINAMIDE (UNII: 25X51I8 RD4)

PANTO THENIC ACID (UNII: 19 F5HK2737)

PYRIDO XINE (UNII: KV2JZ1BI6 Z)

RIBO FLAVIN (UNII: TLM29 76 OFR)

THIAMINE (UNII: X6 6 NSO3N35)

ACACIA (UNII: 5C540 3N26 O)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:370 0 0 -733-

1 in 1 CARTON

0 1/0 1/20 11

0 7/0 1/20 18

50 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

The Procter & Gamble Manufacturing Company

1

50 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

2

NDC:370 0 0 -733-

10 0 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 1/0 1/20 11

0 7/0 1/20 18

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph final

pa rt358 H

0 1/0 1/20 11

0 7/0 1/20 18

Labeler -

T he Procter & Gamble Manufacturing Company (004238200)

Revised: 3/2017