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NUTRIXYL ANTI-DANDRUFF

Medically reviewed on September 19, 2017

Dosage form: liquid
Ingredients: SALICYLIC ACID 20mg in 1mL
Labeler: APOLLO HEALTH AND BEAUTY CARE
NDC Code: 63148-450

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 FACTS

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

NUTRIXYL  ANTI-DANDRUFF
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-450
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) 
COCO MONOETHANOLAMIDE 
SODIUM COCOYL SARCOSINATE 
GLYCOL DISTEARATE 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) 
SODIUM CHLORIDE 
SODIUM HYDROXIDE 
EDETATE SODIUM 
BUTYLATED HYDROXYTOLUENE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:63148-450-07207 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H09/18/2014
Labeler - APOLLO HEALTH AND BEAUTY CARE (201901209)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(63148-450)

 
APOLLO HEALTH AND BEAUTY CARE

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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