Label: CLUB WIPES USA SANITIZING WIPES- benzalkonium chloride cloth
- NDC Code(s): 80976-102-01
- Packager: Bubble Marketing LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 17, 2024
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- Drug Facts
- Active ingredient
- Purpose
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- Inactive ingredients
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SPL UNCLASSIFIED SECTION
KILLS 99.99% OF GERMS*
Moisturizing with Aloe and Vitamin E
• Pre-moistened wipes that clean and sanitize
• For use in fitness clubs, medical facilities, schools, and more
• Board-certified dermatologist tested and approved as non-irritating for skin
Manufactured for:
BUBBLE MARKETINGP.O. Box 19121 • Topeka, KS 66619
Tel: 785.862.0340 • Fax: 785.862.0347
www.clubwipesusa.com
DIRECTIONS FOR DISPENSING: Cut small "V" out of the bag and pull Styrofoam® core out of the center of the roll. Pull the first towel from the center of the roll approximately 6 to 8 inches. Place bag in the dispenser and at the same time feed the first towel through the opening on the dispenser.
DISPOSAL: Offer empty container for recycling. If recycling is not available, discard container in trash. Discard towel in trash after use. Do not flush.
CAUTION:
May irritate eyes. See side panel for further precautions and first aid instructions. - Packaging
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INGREDIENTS AND APPEARANCE
CLUB WIPES USA SANITIZING WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80976-102 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) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80976-102-01 1250 in 1 BAG 09/30/2022 1 3.15 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 Drug 505G(a)(3) 09/30/2022 Labeler - Bubble Marketing LLC (079629047)