Nioxin Scalp Treatment System 6 description, usages, side effects, indications, overdosage, supplying and lots more!

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Nioxin Scalp Treatment System 6

Procter & Gamble Manufacturing Company

NIOXIN SCALP TREATMENT 6


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DIRECTIONS

APPLY EVENLY TO ENTIRE SCALP BEFORE SUN EXPOSURE AND AS NEEDED. DO NOT RINSE. CHILDREN UNDER 6 MONTHS OF AGE, CONSULT A DOCTOR.

WARNINGS

FOR EXTERNAL USE ONLY. NOT TO BE SWALLOWED. AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. MAY CAUSE TEMPORARY REDNESS.

STOP USE AND ASK A DOCTOR IF RASH OR IRRITATION DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN.

ACTIVE INGREDIENTS

ENSULIZOLE 4%, SULISOBENZONE 1.6%

INACTIVE INGREDIENTS

WATER, POLYSORBATE 20, SODIUM HYDROXIDE, PHENOXYETHANOL, PEG-12 DIMETHICONE, CITRIC ACID, COCAMIDOPROPYL BETAINE, ACETAMIDE MEA, ISOPROPYL C12-15-PARETH-9 CARBOXYLATE, METHYLPARABEN, TETRASODIUM EDTA, HYDROLYZED KERATIN, PROPYLENE GLYCOL, PROPYLPARABEN, METHYL NICOTINATE, FRAGRANCE, POLYSORBATE 80, POLYSORBATE 60, MENTHA PIPERITA (PEPPERMINT) OIL, MENTHOL, MENTHA ARVENSIS LEAF OIL, PEG-23M, METHYLISOTHIAZOLINONE, CAMELLIA SINENSIS LEAF EXTRACT, HYDROLYZED SILK, LECITHIN, ALEURITES MOLUCCANA SEED OIL, FOENICULUM VULGARE (FENNEL) FRUIT EXTRACT, SACCHAROMYCES/MAGNESIUM FERMENT, BIOTIN/FOLIC ACID/CYANOCOBALAMIN/NIACINAMIDE/PANTOTHENIC ACID/PYRIDOXINE/RIBOFLAVIN/THIAMINE/YEAST POLYPEPTIDES, YEAST EXTRACT, SACCHAROMYCES/IRON FERMENT, SACCHAROMYCES/COPPER FERMENT, SACCHAROMYCES/SILICON FERMENT, SACCHAROMYCES/ZINC FERMENT.

DISTR. BY
THE WELLA CORPORATION,
WOODLAND HILLS, CA 91367

Questions?

1-800-935-5273 (US)

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

NIOXIN®

SCALP TREATMENT®
SPF 15 SUNSCREEN

medium to coarse hair

NOTICEABLY THINNING

CHEMICALLY TREATED

6

100 mL (3.38 FL OZ)

Nioxin Scalp Treatment System 6

Nioxin Scalp Treatment System 6

Ensulizole and Sulisobenzone LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37000-738
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Ensulizole Ensulizole 41.2 mg
SULISOBENZONE 16.48 mg

Inactive Ingredients

Ingredient Name Strength
water
POLYSORBATE 20
SODIUM HYDROXIDE
PHENOXYETHANOL
PEG-12 DIMETHICONE (300 CST)
CITRIC ACID MONOHYDRATE
COCAMIDOPROPYL BETAINE
ACETIC MONOETHANOLAMIDE
METHYLPARABEN
EDETATE SODIUM
propylene glycol
PROPYLPARABEN
METHYL NICOTINATE
polysorbate 80
POLYSORBATE 60
PEPPERMINT OIL
MENTHOL
MENTHA ARVENSIS LEAF OIL
METHYLISOTHIAZOLINONE
GREEN TEA LEAF
POLYETHYLENE GLYCOL 1000000
KUKUI NUT OIL
FENNEL SEED
BIOTIN
FOLIC ACID
Cyanocobalamin
NIACINAMIDE
PANTOTHENIC ACID
PYRIDOXINE
RIBOFLAVIN
Thiamine
yeast

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 100 in 1 BOTTLE, PLASTIC
2 200 in 1 BOTTLE, PLASTIC
3 40 in 1 BOTTLE, PLASTIC
4 NDC:37000-738-40 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-05-01


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