LETHECHNIQ DANDRUFF MOISTURIZING- selenium sulfide shampoo

LeThechniq Dandruff by

Drug Labeling and Warnings

LeThechniq Dandruff by is a Otc medication manufactured, distributed, or labeled by HY-VEE, Inc, Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Selenium Sulfide 1%

Purpose

Anti-Dandruff

Uses

For relief of flaking, and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of re-occurence

Warnings

For external use only

Ask a doctor before using if you have

Seborrheic dermatitis in areas other than the scalp

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

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

• Shake well, apply shampoo, rinse thoroughly
• For best results, use at least twice a week or as directed by a doctor
  

Other information

Store at room temperature

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

LETHECHNIQ DANDRUFF  MOISTURIZING
selenium sulfide shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42507-611
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: 42507-611-11	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 - HY-VEE, Inc (006925671)

Registrant - Apollo Health and Beauty Care (201901209)

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