EQUATE MOISTURIZING DANDRUFF- selenium sulfide liquid 
WAL-MART STORES INC

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.

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DRUG FACTS

Active ingredient

Selenium Sulfide 1%

Purpose

Anti-Dandruff/Anti-Seborrheic Dermatitis

Uses

For the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.

Warnings

For external use only.

Ask a doctor if you have

seborrheic dermatitis in areas other than the scalp.

When using this product

  • Avoid contact with eyes
  • if contact occurs, rinse eyes thoroughly with water
  • may stain 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

Other information

store at room temperature

Inactive ingredients

Water (Aqua), Sodium Laureth Sulfate, Distearyl Phthalic Acid Amide, Sodium Chloride, Cocamidopropyl Betaine, Sodium Stearoyl Lactylate, Dimethicone, DMDM Hydantoin, Citric Acid, Fragrance (Parfum), Sodium Hydroxide, Sodium Citrate, Aloe Barbadensis Leaf Juice, Hydroxypropyl Methylcellulose, Titanium Dioxide (CI 77891), Blue 1 (CI 42090).

Questions?

Call: 1-888-287-1915

Label Copy

Image of the label

EQUATE  MOISTURIZING DANDRUFF
selenium sulfide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-522
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
DISTEARYL PHTHALAMIC ACID (UNII: 5552GSZ9LI)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-522-12325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H11/23/2015
Labeler - WAL-MART STORES INC (051957769)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(49035-522)

Revised: 11/2015
Document Id: 4006a712-42b6-432b-a961-ab58eefc7135
Set id: 738d33ef-27f3-45e5-adb8-f41345abbbb3
Version: 2
Effective Time: 20151124
 
WAL-MART STORES INC