GOLD ANTIBACTERIAL HAND- chloroxylenol soap

Gold Antibacterial Hand by

Drug Labeling and Warnings

Gold 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 Ingredients Purpose

Chlorxylenol 0.3% Antibacterial

PURPOSE

Uses For hand washing to decrease bacteria on the skin

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Stop use and ask a doctor if irritation and redness develops.

WARNINGS

Warnings

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush with water.

DOSAGE & ADMINISTRATION

Directions

• wet hands as needed
• lather vigourously for at least 15 seconds
• rinse and dry thoroughly

INACTIVE INGREDIENT

Inactive ingredients Water, sodium laureth sulfate, cocamidopropyl betaine, sodium laureth sulfate, sodium chloride, fragrance, citric acid, PEG-150 distearate, methylchloroisothiazolinone, methylisothiazolinone, FD&C Yellow No. 5, D&C red No. 33

PRINCIPAL DISPLAY PANEL

Safety

Gold Antibacterial Hand Soap

15 FL OZ. (444 mL)

INGREDIENTS AND APPEARANCE

GOLD ANTIBACTERIAL HAND 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-584
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-584-01	444 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/08/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/08/2018

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(22431-584)