Safety Gold Antibacterial Hand 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]

SAFETY GOLD ANTIBACTERIAL HAND- benzalkonium chloride soap 
Blue Cross Laboratories

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Safety Gold Antibacterial Hand Soap

Active Ingredient Purpose

Benzalkonium Chloride 0.13% Antibacterial

Uses for hand washing to decrease bacteria on the skin

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

Stop use and ask a doctor if irritation and redness develops

Warnings

For external use only

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

Directions

• Wet hands as needed
• Lather vigorously for at least 15 seconds
• rinse and dry thoroughly

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

Safety Gold

Antibacterial Hand Soap

Kills Germs

Cleans & Softens Hands

16 FL OZ (473 mL)

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	04/07/2023
2	NDC: 22431-586-02	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/26/2020	04/07/2023
3	NDC: 22431-586-03	1180 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020	04/07/2023
4	NDC: 22431-586-04	444 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020	04/07/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	08/26/2020	04/07/2023

Labeler - Blue Cross Laboratories (118887378)

Revised: 6/2025

Document Id: 387e4381-622d-1a64-e063-6294a90a4e73

34390-5

Set id: adcb592f-84fc-2282-e053-2995a90abd2a

Version: 3

Effective Time: 20250626