ANTIMICROBIAL FOAMING HAND- benzalkonium chloride soap

Antimicrobial Foaming Hand by

Drug Labeling and Warnings

Antimicrobial Foaming Hand by is a Otc medication manufactured, distributed, or labeled by Health Technology Professional Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each use)

Benzalkonium Chloride .13%

Purpose

Antimicrobial

Uses

For hand washing to decrease bacteria on the skin.

Warnings

For external use only

When using this product

Avoid contact with eyes. In case of contact flush eyes with water. Do not ingest,

Stop use and ask a doctor if

irritation or redness develop or condition persists.

Keep Out Of Reach Of Children

If swallowed get medical help or contact a Poison Control Center immediately.

Directions

Apply to wet hands. Work into a lather and rinse thoroughly.

Other Information

Store between 40ºF and 120ºF

Inactive ingredinets

Water, Cocamidopropyl Betaine,Glycerine, Caprylyl Glucoside, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Fragrance, Citric Acid, Aloe Vera, Yellow #5, Red #40

PRINCIPAL DISPLAY PANEL

Sample

16 oz

1 Gallon

INGREDIENTS AND APPEARANCE

ANTIMICROBIAL FOAMING HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81775-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C RED NO. 40 (UNII: WZB9127XOA)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)

Product Characteristics
Color	orange (Orange Liquid)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81775-100-01	50.28 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/30/2022
2	NDC: 81775-100-02	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/30/2022
3	NDC: 81775-100-03	3785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2022

Labeler - Health Technology Professional Products, Inc (622285547)

Registrant - Health Technology Professional Products, Inc (622285547)