CVS HEALTH ANTIBACTERIAL MOIST HAND WIPES- benzalkonium chloride solution

CVS Health Antibacterial Moist Hand Wipes by

Drug Labeling and Warnings

CVS Health Antibacterial Moist Hand Wipes by is a Otc medication manufactured, distributed, or labeled by CVS PHARMACY, INC, Jianerkang Medical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride  0.13%

Purpose

Antiseptic

Use

To decrease bacteria on the skin

Warnings

For external use only

WHEN USING

• When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin

STOP USE

Stop use and ask a doctor if irritation and redness develop, condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Apply to hands
• Allow to dry without wiping
• For children under 6, use only under adult supervision
• Not recommended for infants

Other information

• Keep containers tightly closed in a dry, cool and well ventilated place
• Recommended storage temperature: 32F to 104F (0C to 40C)

Inactive ingredients

Aloe Barbadensis Leaf Juice, Dodecyl (ethylbenzyl) Dimethylammonium Chloride, Ethylhexylglycerin, Fragrance, Phenoxyethanol, Propylene Glycol, Sodium Citrate, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS HEALTH ANTIBACTERIAL MOIST HAND WIPES 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-001
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 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-001-01	20 in 1 BAG	05/27/2021
1		4.3 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/27/2021

Labeler - CVS PHARMACY, INC (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Jianerkang Medical Co., Ltd		530968767	manufacture(51316-001)