MULTI-PURPOSE ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth

Multi-purpose Antibacterial Wet Wipes by

Drug Labeling and Warnings

Multi-purpose Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by NUVOMED,INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial Agent

Use

Decreases bacteria on skin.

Warnings

For external use only.

Do not use

Do not use if you are allergic to any of the ingredients.

WHEN USING

Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash develops and continues 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

Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.

Other information

The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.

Inactive ingredients

C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

MULTI-PURPOSE ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78927-003
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
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78927-003-01	77 g in 1 BAG; Type 0: Not a Combination Product	06/13/2020
2	NDC: 78927-003-02	295 g in 1 BAG; Type 0: Not a Combination Product	06/13/2020
3	NDC: 78927-003-03	435 g in 1 PAIL; Type 0: Not a Combination Product	06/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/13/2020

Labeler - NUVOMED,INC. (080809709)