MEDICATED DANDRUFF- selenium sulfide shampoo

Medicated Dandruff by

Drug Labeling and Warnings

Medicated Dandruff by is a Otc medication manufactured, distributed, or labeled by Target Corp, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Selenium sulfide 1%

Purpose

Antidandruff

Use

for relief of itching and flaking associated with dandruff and seborrheic dermatitis and to help prevent reoccurrence

Warnings

For external use only

Ask a Doctor

before use if you have seborrheic dermatitis in areas other than the scalp

When using this product

• do not get into 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 as directed

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

• shake well
• wet hair, massage onto scalp, rinse thoroughly
• for best results use at least twice a week or as directed by a doctor

Other information

for color-treated or permed hair, rinse extra thoroughly

Inactive ingredients

water, ammonium lauryl sulfate, ammonium laureth sulfate, TEA-lauryl sulfate, cocamidopropyl betaine, magnesium aluminum silicate, fragrance, menthol, cocamide MEA, DMDM hydantoin, citric acid, hydroxypropyl methylcellulose, sodium citrate, sodium chloride, xanthan gum, cellulose gum, blue 1, red 33

Disclaimer

This producty is not manufactured or distributed by Chattem, Inc., distributor of Selsun Blue Medicated Dandruff Shampoo

Questions?

Call 1-800-910-6874

Adverse reactions

Dist. by Target Corp., Mpls., MN55403

Made in U.S.A.

Shop Target.com

246.002/246AE

principal display panel

Medicated

Shampoo

Selenium Sulfide

Dandruff Shampoo

Compare to Selsum Blue

Dandruff control shampoo

maximum medicated control

Scalp-tastic

UP & UP

11 FL OZ (325 mL)

INGREDIENTS AND APPEARANCE

MEDICATED DANDRUFF 
selenium sulfide shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-246
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (selenium sulfide - UNII:Z69D9E381Q)	SELENIUM SULFIDE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
AMMONIUM LAURETH-12 SULFATE (UNII: E1ZP93931S)
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
MENTHOL (UNII: L7T10EIP3A)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYPROMELLOSES (UNII: 3NXW29V3WO)
XANTHAN GUM (UNII: TTV12P4NEE)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-246-39	325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/15/1990

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	02/15/1990

Labeler - Target Corp (006961700)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(11673-246)