CLEAR MEN 2 IN 1 COMPLETE CARE ANTIDANDRUFF- pyrithione zinc shampoo

Clear by

Drug Labeling and Warnings

Clear by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a Unilever, Unilever Supply Chain Co. d/b/a Unilever, Marietta Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Pyrithione Zinc (1.0%)

PURPOSE

Purpose

Anti-Dandruff

INDICATIONS & USAGE

Use Helps prevent and control recurrence of itching and flaking associated with dandruff

WARNINGS

Warnings
For external use only

When using this product Avoid contact with 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 of this product as directed.

Keep this and all drugs out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions Wet hair, massage into scalp, rinse.  Repeat if desired.  For best results use at least twice a week or as directed by a doctor.

INACTIVE INGREDIENT

Inactive Ingredients

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Dimethiconol, Carbomer, Dimethicone, DMDM Hydantoin, Guar Hydroxypropyltrimonium Chloride, Citric Acid, Zinc Sulfate, TEA-Dodecylbenzenesulfonate, Poloxamer 407, Laureth-23, Butylene Glycol, Laureth-4, Lysine HCl, Tocopheryl Acetate, Panthenol, PPG-9, Iodopropynyl Butylcarbamate, PEG-4, Xanthan Gum, Helianthus Annuus (Sunflower) Seed Oil, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Glycine Soja (Soybean) Oil, Cocos Nucifera (Coconut) Oil, Methylchloroisothiazolinone, Methylisothiazolinone, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Panax Ginseng Root Extract, Mentha Viridis (Spearmint) Leaf Oil.

QUESTIONS

Questions, comments? 1-800-372-6389

21.9 FL OZ

PDP back

INGREDIENTS AND APPEARANCE

CLEAR  MEN 2 IN 1 COMPLETE CARE ANTIDANDRUFF
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1269
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Pyrithione Zinc (UNII: R953O2RHZ5) (Pyrithione Zinc - UNII:R953O2RHZ5)	Pyrithione Zinc	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
XANTHAN GUM (UNII: TTV12P4NEE)
DMDM HYDANTOIN (UNII: BYR0546TOW)
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PPG-9 (UNII: I29VQH0G0B)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SPEARMINT OIL (UNII: C3M81465G5)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
ZINC SULFATE (UNII: 89DS0H96TB)
DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLOXAMER 407 (UNII: TUF2IVW3M2)
LAURETH-23 (UNII: N72LMW566G)
LAURETH-4 (UNII: 6HQ855798J)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ALMOND OIL (UNII: 66YXD4DKO9)
POLYETHYLENE GLYCOL 400000 (UNII: 439X29GCJZ)
PANTHENOL (UNII: WV9CM0O67Z)
LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
SOYBEAN OIL (UNII: 241ATL177A)
ASIAN GINSENG (UNII: CUQ3A77YXI)
TEA TREE OIL (UNII: VIF565UC2G)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1269-1	381 mL in 1 CONTAINER; Type 0: Not a Combination Product
2	NDC: 64942-1269-2	975 mL in 1 CONTAINER; Type 0: Not a Combination Product
3	NDC: 64942-1269-3	647 mL in 1 CONTAINER; Type 0: Not a Combination Product
4	NDC: 64942-1269-4	476 mL in 1 CONTAINER; Type 0: Not a Combination Product
5	NDC: 64942-1269-5	89 mL in 1 CONTAINER; Type 0: Not a Combination Product
6	NDC: 64942-1269-6	50 mL in 1 CONTAINER; Type 0: Not a Combination Product
7	NDC: 64942-1269-7	8.3 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	12/15/2015

Labeler - Conopco Inc. d/b/a Unilever (001375088)

Establishment
Name	Address	ID/FEI	Business Operations
Unilever Supply Chain Co. d/b/a Unilever		043510056	manufacture(64942-1269)

Establishment
Name	Address	ID/FEI	Business Operations
Marietta Corp		111359712	manufacture(64942-1269)

Establishment
Name	Address	ID/FEI	Business Operations
Marietta Corp		010765394	manufacture(64942-1269)