CLEAR ANTIBACTERIAL HAND- triclosan soap

Clear Antibacterial Hand by

Drug Labeling and Warnings

Clear Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories, Inc, Ningbo Liyuan Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient             Purpose

Triclosan  0.15%           Antibacterial

Uses for hand washing to decrease to decrease bacteria on the skin

Keep out of reach of children If swallowed, get medical help or contactor contact a Poison Control Center.

Stop use and ask a doctor if irritation and redness develops

Warnings

For external use only

Directions

wet hands as needed

lather vigorously for at least 15 seconds

rinse and dry

water (aqua), sodium laureth sulfate, ammonium lauryl sulfate, decyl glucoside, cocamidopropyl betaine, glycerin, sodium chloride, PEG-18 glyceryl oleate/cocoate, fragrance, DMDM hydantoin, tetrasodium EDTA, citric acid, FD&C blue 1, D&C red 33.

PRINCIPAL DISPLAY PANEL

Safety

Clear Antibacterials Hand Soap

15 FL OZ. 444mL

INGREDIENTS AND APPEARANCE

CLEAR ANTIBACTERIAL HAND 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-582
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	.15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-18 GLYCERYL OLEATE/COCOATE (UNII: VD2D270332)
DMDM HYDANTOIN (UNII: BYR0546TOW)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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: 22431-582-01	444 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/25/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/25/2014

Labeler - Blue Cross Laboratories, Inc (008298879)

Registrant - Blue Cross Laboratories, Inc (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(22431-582)