MEDICATED DANDRUFF- selenium sulfide 1% shampoo

Medicated Dandruff by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Selenium sulfide 1%

Purpose

Anti-Dundruff

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

Stop use and ask a doctor if

condition worsens or does not improve after regular use as directd

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

Adverse Reactions

DISTRIBUTED BY SUPERVALU INC.

EDEN PRAIRIE, MN 55344 USA

Contact us at 1-877-932-7948, or www.supervalu-ourownbrands.com

246.002/246AE

principal display panel

EQUALINE

compare to Selsun Blue active ingredient

Medicated

Dandruff Shampoo

with Menthol

Selenium Sulfide 1%

Maximum medicated control

Healthier hair, healthier scalp

11 FL OZ (325 mL)

INGREDIENTS AND APPEARANCE

MEDICATED DANDRUFF 
selenium sulfide 1% shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-952
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 MONOETHANOLAMIDE (UNII: C80684146D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
XANTHAN GUM (UNII: TTV12P4NEE)
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: 41163-952-39	325 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package	01/19/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	01/19/2015

Labeler - SUPERVALU INC. (006961411)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(41163-952)