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Dandruff

Drug Facts

FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient

Purpose

Uses

Use
Warnings
For external use onlyWhen using this product

Stop use and ask a doctor if
Keep out of reach of children.

Directions

Inactive ingredients

Satisfaction guaranteed
or your money back.
Manufactured For Your Military Exchanges By:
Vi-Jon 8515 Page Avenue
St. Louis, MO 63114

Dandruff

Dandruff LOTION/SHAMPOO

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:55301-311
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC		1 kg

Inactive Ingredients
Ingredient Name	Strength
water
water
SODIUM LAURETH SULFATE
SODIUM LAURYL SULFATE
ZINC CARBONATE
GLYCOL DISTEARATE
CETYL ALCOHOL
SODIUM BENZOATE
MAGNESIUM CARBONATE HYDROXIDE
BENZYL ALCOHOL
SODIUM CHLORIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
SODIUM XYLENESULFONATE
TRIDECETH-12
CETRIMONIUM CHLORIDE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:55301-311-15	.42 in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
partH	part358H	2004-07-09

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!

Dandruff description, usages, side effects, indications, overdosage, supplying and lots more!

Dandruff

Drug Facts

FULL PRESCRIBING INFORMATION

Active ingredient

Purpose

Uses

Dandruff

Product Information

Active Ingredient/Active Moiety

Inactive Ingredients

Packaging

Marketing Information