Label: DIAMOND WIPES ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth
- NDC Code(s): 64709-111-10
- Packager: Diamond Wipes International Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 9, 2024
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- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
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Principal Display Panel
Diamond wipes®
Do Not Flush
99.9% EFFECTIVE against most common germs*
1 Wipe| Antibacterial Hand Wipes
Made in U.S.A. with global components
Aloe Vera & Vitamin E
Cleans & Sanitizes
Drug Facts
Active ingredient Purpoe
Benzalkonium Chloride 0.13% w/w.................. Antimicrobial
Uses ■for hand sanitizing to decrease bacteria on skin ■recommended for repeated use
Warnings
■ For external use only ■When using this product avoid contact with eyes. ■Stop use and contact a doctor If irritation or redness persists for more than 72 hours ■Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.
Directions ■open packet ■remove and unfold wipe ■wipe hands thoroughly ■do not flush
Inactive ingredients Alcohol Denat., Aloe Barbadensis Leaf Juice, Citric Acid, Fragrance, Polysorbate 20, Sorbic Acid, Tocopheryl Acetate, Water
*Escherichia coli, Staphylococcus aureus, Salmonella typhimurium, Pseudomonas aeruginosa, Burkholderia cepacia, Enterobacter cloacae, Enterococcus faecalis, Streptococcus pyogenes, Candida albicans, Aspergillus brasiliensis
7 66670 01637 5
Reorder Item# F1637
Diamond Wipes Int’l Inc.
Chino, CA 91710
(800) 454-1077
diamondwipes.com
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INGREDIENTS AND APPEARANCE
DIAMOND WIPES ANTIBACTERIAL HAND WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64709-111 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) SORBIC ACID (UNII: X045WJ989B) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POLYSORBATE 20 (UNII: 7T1F30V5YH) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64709-111-10 1 g in 1 PACKET; Type 0: Not a Combination Product 01/01/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/01/2010 Labeler - Diamond Wipes International Inc. (161104729)