SAFETY GOLD ANTIBACTERIAL HAND- benzalkonium chloride soap

Safety Gold Antibacterial Hand by

Drug Labeling and Warnings

Safety Gold Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Blue Cross Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Benzalkonium Chloride 0.13% 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 vigorously for at least 15 seconds
• rinse and dry thoroughly

INACTIVE INGREDIENT

Inactive ingredients Water(aqua), Sodium Laureth Sulfate, Sodium Chloride, DMDM Hydantoin, Fragrance, Citric Acid, D&C Orange #4, D&C Yellow #10

PRINCIPAL DISPLAY PANEL

Safety Gold

Antibacterial Hand Soap

Kills Germs

Cleans & Softens Hands

16 FL OZ (473 mL)

INGREDIENTS AND APPEARANCE

SAFETY GOLD ANTIBACTERIAL HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-586
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
WATER (UNII: 059QF0KO0R)
DMDM HYDANTOIN (UNII: BYR0546TOW)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-586-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/26/2020
2	NDC: 22431-586-02	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/26/2020
3	NDC: 22431-586-03	1180 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
4	NDC: 22431-586-04	444 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/26/2020

Labeler - Blue Cross Laboratories (008298879)