HIMARK- benzalkonium chloride liquid

HIMark by

Drug Labeling and Warnings

HIMark by is a Otc medication manufactured, distributed, or labeled by Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

Helps eliminate bacteria on hands

Warnings

For External Use only

When using this product

• Avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor if

Stop use and ask a doctor if

• irritation or redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

• From Liquid Hand Soap pump bottle, apply onto wet hands
• Lather and rinse thoroughly.

Other Information

Store at room Temperature.

Inactive Ingredients

Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40 (CI 16035), Yellow 5(CI19140), Red 33 (CI17200).

Questions

1-866-795-8481

Principal Display Panel- 50 Oz

Principal Display Panel-7.5 Oz

INGREDIENTS AND APPEARANCE

HIMARK 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63148-401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	130 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C RED NO. 40 (UNII: WZB9127XOA)
BASIC YELLOW 5 (UNII: 07BP340B4T)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM SULFATE (UNII: 0YPR65R21J)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63148-401-07	221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2023
2	NDC: 63148-401-50	1478 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/01/2023

Labeler - Apollo Health and Beauty Care (201901209)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture(63148-401)