CVS PHARMACY DANDRUFF MOISTURIZING WITH ALOE- selenium sulfide shampoo

CVS Pharmacy Dandruff by

Drug Labeling and Warnings

CVS Pharmacy Dandruff by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy Inc, Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Selenium Sulfide 1%

Purpose

Anti-Dandruff

Uses

Controls flaking, scaling and itching associated with dandruff

Warnings

For external use only

Do Not Use

• On scalp that is broken or inflamed.
  
• If you are allergic to ingredients in this product
  

When using this product

avoid contact with eyes. If contact occurs, rinse with water. For use on color treated or permed hair, rinse thoroughly

Stop using this product and ask doctor if

• rash appears
• condition worsens or does not improve in 2-4 weeks
  

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

If pregnant or breast feeding

ask a doctor before use

Directions

• Adults and children 12 years and over: wet hair thoroughly, apply shampoo, generously lather, rinse thoroughly. Repeat. Use every 3-4 days for up to 8 weeks or as directed by a doctor. Then use only as needed to control dandruff.
• Children under 12 years: ask a doctor
  

Other Information

• store between 35o and 85o F (2o and 30oC)
• protect from freezing
• see bottom of bottle for lot number and expiration date
  

Inactive Ingredients

Water (Aqua), Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Dihydrogenated Tallow Phthalic Acid Amide, Cocamide DEA, Fragrance (Parfum), Titanium Dioxide, Dimethicone, Hydroxypropyl Methylcellulose, Citric Acid, Sodium Isostearoyl Lactylate, DMDM Hydantoin, Aloe Barbadensis Leaf Juice, Sodium Citrate, Sodium Chloride, Blue 1 (CI 42090)

Package Front and Back Labels

ra11.jpg

INGREDIENTS AND APPEARANCE

CVS PHARMACY DANDRUFF  MOISTURIZING WITH ALOE
selenium sulfide shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-611
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM - UNII:H6241UJ22B)	SELENIUM SULFIDE	1 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
DIMETHICONE (UNII: 92RU3N3Y1O)
HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM ISOSTEAROYL LACTYLATE (UNII: 8730J0D3EV)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-611-11	325 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/15/2010

Labeler - CVS Pharmacy Inc (062312574)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture