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Suave Revitalizing Mint and Eucalyptus AntiDandruff Conditioner

Dosage form: suspension
Ingredients: Pyrithione Zinc 0.5mL in 100mL
Labeler: Conopco Inc. d/b/a Unilever
NDC Code: 64942-1236

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.

Suave Revitalizing Mint and Eucalyptus Anti Dandruff Conditioner PDP and drug facts box

Active Ingredient

Pyrithione Zinc (0.5%)

Purpose
Antidandruff

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

Directions: Wet hair, massage onto scalp, rinse.  Repeat if desired.  For best results use at least twice a week or as directed by a doctor.

Inactive Ingredients
Water (Aqua)
Cetearyl Alcohol
Cyclopentasiloxane
Stearamidopropyl Dimethylamine
Dimethiconol
Behentrimonium Chloride
Fragrance (Parfum)
Dipropylene Glycol
Lactic Acid
DMDM Hydantoin
Zinc Sulfate
Sodium Chloride
TEA-Dodecylbenzenesulfonate
PEG-150 Distearate
Helianthus Annuus (Sunflower) Seed Oil
Tocopheryl Acetate
Methylisothiazolinone
Methylchloroisothiazolinone
Mentha Viridis (Spearmint) Leaf Oil
Eucalyptus Globulus Leaf Oil
Yellow 5 (CI 19140)
Blue 1 (CI 42090)

Question (or comments)?: 1-800-782-8301

PDP
SUAVE  REVITALIZING MINT AND EUCALYPTUS ANTIDANDRUFF CONDITIONER
pyrithione zinc suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1236
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Pyrithione Zinc (Pyrithione) Pyrithione Zinc0.5 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CETOSTEARYL ALCOHOL 
CYCLOMETHICONE 5 
SODIUM CHLORIDE 
STEARAMIDOPROPYL DIMETHYLAMINE 
BEHENTRIMONIUM CHLORIDE 
DMDM HYDANTOIN 
TEA-DODECYLBENZENESULFONATE 
DIPROPYLENE GLYCOL 
LACTIC ACID 
ZINC SULFATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
SPEARMINT OIL 
PEG-150 DISTEARATE 
EUCALYPTUS OIL 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
SUNFLOWER OIL 
.ALPHA.-TOCOPHEROL ACETATE, D- 
DIMETHICONOL (41 MPA.S) 
Packaging
#Item CodePackage Description
1NDC:64942-1236-1428 mL in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H02/09/2012
Labeler - Conopco Inc. d/b/a Unilever (001375088)
Establishment
NameAddressID/FEIOperations
Unilever Supply Chain Co. d/b/a Unilever043510056manufacture

Revised: 02/2012
Document Id: e2ad7a1f-c890-4f36-9b02-febc382d0ba1
Set id: f3ba6a7c-2d4b-48f7-9c72-1c0ae45b42b4
Version: 1
Effective Time: 20120209
 
Conopco Inc. d/b/a Unilever

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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