Label: CLUB WIPES USA SANITIZING WIPES- benzalkonium chloride cloth
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NDC Code(s):
80976-101-01,
80976-101-02,
80976-101-03,
80976-101-04, view more80976-101-05
- Packager: Bubble Marketing Llc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 5, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
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- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
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SPL UNCLASSIFIED SECTION
Manufactured for: BUBBLE MARKETING
P.O. Box 19121 • Topeka, KS 66619
Tel: 785.862.0340 • Fax: 785.862.0347
www.clubwipesusa.com
Kills 99.99% of germs
• Wet wipes cleans and sanitizes
• Designed to use in health facilities, health clubs, schools and wherever germs are present
• Board Certified Dermatologist Tested & Approved as a non-sensitizer nor irritant to skin
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.
KEEP OUT OF REACH OF CHILDREN.
- 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:80976-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.12 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:80976-101-05 160 in 1 BAG 12/03/2020 1 3.02 mL in 1 PACKAGE; Type 0: Not a Combination Product 2 NDC:80976-101-04 900 in 1 BAG 12/03/2020 2 3.02 mL in 1 PACKAGE; Type 0: Not a Combination Product 3 NDC:80976-101-03 800 in 1 BAG 12/03/2020 3 3.02 mL in 1 PACKAGE; Type 0: Not a Combination Product 4 NDC:80976-101-02 1000 in 1 BAG 12/03/2020 4 3.02 mL in 1 PACKAGE; Type 0: Not a Combination Product 5 NDC:80976-101-01 1250 in 1 BAG 12/03/2020 5 3.02 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 12/03/2020 Labeler - Bubble Marketing Llc (079629047)