ARMOR ANTIBACTERIAL BODY TREATMENT BENZALKONIUM CHLORIDE- benzalkonium chloride liquid

Armor Antibacterial Body Treatment Benzalkonium Chloride by

Drug Labeling and Warnings

Armor Antibacterial Body Treatment Benzalkonium Chloride by is a Otc medication manufactured, distributed, or labeled by Rida LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antiseptic

Uses

• Helps reduce bacteria that can cause skin infections and odor
• Deeply cleanses and detoxifies clogged pores
• Ideal for acne-prone, oily, and sensitive skin

Warnings

For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water

Stop use and ask a doctorif irritation or redness develops and persists

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

KEEP OUT OF REACH OF CHILDREN

Directions

• Apply to wet skin
• Massage gently into a lather, focusing on problem areas
• Rinse thoroughly
• Use once or twice daily as needed

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Sodium Lauroyl Sarcosinate, Glycerin, Charcoal Powder, Mel (Honey), Aloe Barbadensis Leaf Juice, Niacinamide, Panthenol, Butyrospermum Parkii (Shea) Butter, Chamomilla Recutita Flower Extract, Calendula Officinalis Extract, Cucumis Sativus (Cucumber) Fruit Extract, Tocopheryl Acetate, Allantoin, Citric Acid, Sodium Gluconate, Phenoxyethanol, Ethylhexylglycerin

Questions?

• Store in a cool, dry place
• Dermatologist tested
• Free from parabens, sulfates, artificial dyes, and animal testing
• Best if used within 12 months of opening

Product label

INGREDIENTS AND APPEARANCE

ARMOR ANTIBACTERIAL BODY TREATMENT BENZALKONIUM CHLORIDE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83004-028
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
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LOPERAMIDE (UNII: 6X9OC3H4II)
GLYCERIN (UNII: PDC6A3C0OX)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
HONEY (UNII: Y9H1V576FH)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
NIACINAMIDE (UNII: 25X51I8RD4)
PANTHENOL (UNII: WV9CM0O67Z)
SHEA BUTTER (UNII: K49155WL9Y)
CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CUCUMBER (UNII: YY7C30VXJT)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALLANTOIN (UNII: 344S277G0Z)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM GLUCONATE (UNII: R6Q3791S76)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83004-028-01	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/01/2025

Labeler - Rida LLC (004425803)