Label: NUVIK LARGE ROLL IN BUCKET ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth
- NDC Code(s): 74602-900-80
- Packager: Nuvik Usa, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 18, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
■ in children less than 2 months of age
■ on open skin wounds
■ if you are allergic to any of the ingredients
When using this product
■ do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if
■ irritation and redness develop
■ condition persists for more than 72 hours
- Directions
- Other information
- Inactive Ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
Alcohol-Free Cleaner & Antibacterial
Crocodile Cloth® | www.crocodilecloth.com | Part# 9161
Nuvik Antibacterial Hand Wipes are a generous 8" X 10" and come in a convenient 800-count roll to minimize refills. These hand wipes will clean and deodorized by reducing harmful bacteria.
To Dispense: Look for tear-notch located at the top of the refill pouch. Open pouch by tearing straight across at notch. Starting from the center of the roll, pull one wipe through the pouch center opening and then thread wipe through the dispenser nozzle. Adjust nozzle tension on dispenser, if applicable. For use with upward-pull dispensers (floor stand or wall units) only: product will drip in a downward-pull dispenser.
Ideal for
■ Gyms/Training Centers ■ Pilates and Yoga Centers
■ Clubs ■ Dance Studios
■ Tanning Salons ■ Spin/Cycling Studios
■ Day Spas ■ Medical Facilities
Recyclable packaging
Do not flush used wipes
Manufactured for:
Nuvik USA Inc
Gahanna, Ohio 43230
Made in China
www.nuvikglobal.com
- Packaging
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INGREDIENTS AND APPEARANCE
NUVIK LARGE ROLL IN BUCKET ANTIBACTERIAL HAND WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74602-900 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CHAMOMILE (UNII: FGL3685T2X) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) CHLORPHENESIN (UNII: I670DAL4SZ) N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74602-900-80 1 in 1 PAIL 06/01/2020 1 800 in 1 BAG 1 6.1 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) 06/01/2020 Labeler - Nuvik Usa, Inc. (117472505)

