MANE N TAIL DAILY CONTROL ANTI-DANDRUFF- pyrithione zinc shampoo, suspension

Mane n Tail Daily Control Anti-Dandruff by

Drug Labeling and Warnings

Mane n Tail Daily Control Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by Straight Arrow Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Pyrithione Zinc  1%

PURPOSE

Purpose

Anti-dandruff

INDICATIONS & USAGE

Use -helps prevent recurrence of flaking and itching associated with dandruff.

WARNINGS

Warnings -   For external use only

When using this product

• do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.
  

Stop use and ask a doctor if

• 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.

DOSAGE & ADMINISTRATION

Directions:

• For maximum dandruff control, use every time you shampoo.
• Wet hair, massage onto scalp, rinse, repeat if desired.
• For best results, use at least twice a week or as directed by a doctor.
  

INACTIVE INGREDIENT

Inactive Ingredients:  Aqua (Water), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Coco Glucoside, Acrylates Copolymer, Cocamidopropyl Betaine, Fragrance (Parfum), Sodium Hydroxide, Olea Europaea (Olive) Fruit Oil, Olea Europaea (Olive) Leaf Extract, Herbal Extract Blend:  Equisetum Arvense (Horsetail) Leaf Extract, Larrea Divaricata (Chaparral) Extract, Tussilago Farfara (Coltsfoot) Flower Extract, Aesculus Hippocastanum (Horse Chestnut) Seed Extract, Spiraea Ulmaria (Meadowsweet) Flower Extract, Trifolium Pratense (Clover) Flower Extract, PEG-8 Amodimethicone, Methylchloroisothiazolinone/Methylisothiazolinone, Blue #1 (CI 42090), Yellow #5 (CI 19140).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MANE N TAIL DAILY CONTROL ANTI-DANDRUFF 
pyrithione zinc shampoo, suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62001-0319
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	.01 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIMETHICONE (UNII: 92RU3N3Y1O)
COCOA BUTTER (UNII: 512OYT1CRR)
LAURETH-4 (UNII: 6HQ855798J)
LAURETH-7 (UNII: Z95S6G8201)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALMOND OIL (UNII: 66YXD4DKO9)
OLIVE OIL (UNII: 6UYK2W1W1E)
EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
LARREA TRIDENTATA TOP (UNII: PK0TXD049P)
TUSSILAGO FARFARA (UNII: 0JXZ63016V)
HORSE CHESTNUT (UNII: 3C18L6RJAZ)
FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
RED CLOVER (UNII: L9153EKV2Y)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62001-0319-1	7257.6 g in 1 BOTTLE, PLASTIC
2	NDC: 62001-0319-2	453.6 g in 1 POUCH
3	NDC: 62001-0319-3	158.76 g in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	04/20/2008

Labeler - Straight Arrow Products, Inc. (061580593)

Registrant - Straight Arrow Products, Inc. (061580593)

Establishment
Name	Address	ID/FEI	Business Operations
Straight Arrow Products, Inc.		061580593	manufacture