1200 WET WIPES- benzalkonium chloride cloth

1200 Wet Wipes by

Drug Labeling and Warnings

1200 Wet Wipes by is a Otc medication manufactured, distributed, or labeled by D D Office Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benzalkonium Chloride 0.10%

Purpose

Sanitizing

Use

hand sanitizer to decrease bacteria on the skin.

Warnings

For external use only. 

Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.

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

Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

Keep out of reach of children unless under adult supervision. 

If swallowed, get medical help

DOSAGE & ADMINISTRATION

Direction

Wet hands thoroughly with product and allow to dry without wiping.

Additional Information:

Store below 110°F (43°C).

May discolor certain fabrics or surfaces.

Inactive ingredients

Sodium Carboxymethyl Lauryl Glucoside, Sodium PCA, Cocamide DEA, Citric Acid, Parfum / Fragrance, Ethyl glycerin, Vitamin E, Water, Aloe Essence Extract, Phenoxyethanol

SPL UNCLASSIFIED SECTION

Distributed by DD Office Products, Inc.

Los Angeles, CA | www.libertypp.com

Made in China

Packaging

INGREDIENTS AND APPEARANCE

1200 WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77081-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77081-001-12	1200 in 1 BAG	07/15/2020
1		3.5 mL in 1 PACKAGE; 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	07/15/2020

Labeler - D D Office Products, Inc. (023854701)