DISCOUNT DRUG MART- benzalkonium chloride liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

Helps decrease 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

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 pump bottle, apply onto wet hands. Lather and rinse thoroughly.

Inactive ingredients

Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Sodium Sulfate, Fragrance (Parfum), Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5 (Cl 19140), Red 4 (CI 14700)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DISCOUNT DRUG MART 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63148-146
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
COCAMIDE MEA (UNII: C80684146D)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
WATER (UNII: 059QF0KO0R)
YELLOW 5 (UNII: I753WB2F1M)
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
TETRASODIUM EDTA (UNII: MP1J8420LU)
RED 4 (UNII: X3W0AM1JLX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
SODIUM SULFATE (UNII: 0YPR65R21J)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63148-146-52	1540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/28/2026
2	NDC: 63148-146-11	325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/28/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/28/2026

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(63148-146)