NUTRIXYL ANTI-DANDRUFF- salicylic acid liquid

NUTRIXYL by

Drug Labeling and Warnings

NUTRIXYL by is a Otc medication manufactured, distributed, or labeled by APOLLO HEALTH AND BEAUTY CARE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

SALICYLIC ACID 2%

PURPOSE

ANTI-DANDRUFF/ANTI-SEBORRHEIC DERMATITIS/ANTI-PSORIASIS

USES

CONTROLS THE SYMPTOMS OF DANDRUFF, SEBORRHEIC DERMATITIS, AND PSORIASIS

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. FOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY

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

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

DIRECTIONS

• FOR BEST RESULTS, USE TWICE A WEEK OR AS DIRECTED BY A DOCTOR
• WET HAIR, MASSAGE ONTO SCALP FOR SEVERAL MINUTES, AND THEN RINSE
• REPEAT IF DESIRED

INACTIVE INGREDIENTS

WATER (AQUA), SODIUM LAURETH SULFATE, ACRYLATES CROSSPOLYMER-4, COCAMIDE MEA, SODIUM COCOYL SARCOSINATE, GLYCOL DISTEARATE, POLYQUATERNIUM-7, FRAGRANCE (PARFUM), SODIUM CHLORIDE, SODIUM HYDROXIDE, TETRASODIUM EDTA, BHT, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, BLUE 1 (CI 42090)

QUESTIONS OR COMMENTS?

1-866-695-3030

LABEL COPY

INGREDIENTS AND APPEARANCE

NUTRIXYL  ANTI-DANDRUFF
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63148-450
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE SODIUM (UNII: MP1J8420LU)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63148-450-07	207 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	09/18/2014

Labeler - APOLLO HEALTH AND BEAUTY CARE (201901209)

Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
APOLLO HEALTH AND BEAUTY CARE		201901209	manufacture(63148-450)