Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride swab
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Contains inactivated NDC Code(s)
NDC Code(s): 40055-0938-2 - Packager: Global Marketing Resources, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 December 9, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Direction for dispensing:
Remove lid from canister.
Lift flap in center of lid.
Pull up corner of center sheet, twist to a point and thread through dispenser hole in lid.
Do not push finger through opening.
Replace lid and pull sheet out at an angle. The next sheet pops up automatically.
when finished reseal by closing lid flap to retain moisture.
Direction for use:
Thoroughly wipe hands and face as desired.
Allow to dry without wiping.
Discard wipe in trash receptacle after use. Do not flush.
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
Convenient Easy to use and carry anytime!
Clean-Up Use to wash up quickly when soap and water are not available
Moisturize soothes and softens dry skin.
Antibacterial Wet Wipes contain soothing Aloe to help moisturize your skin and leave it feeling soft and smooth. Our Wet Wipes are thick and strong to help even the roughest skin.
Distributed by:
Greenbrier International, Inc.
Chesapeake, VA 23320
Made in China
50% More Free
Antibacterial Wet Wipes
Hands and Face Moisturizing Towelettes
with Aloe
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ANTIBACTERIAL WET WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:40055-0938 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.115 mL in 100 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETIC ACID (UNII: 9G34HU7RV0) SORBITOL (UNII: 506T60A25R) ALOE (UNII: V5VD430YW9) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:40055-0938-2 101.6 mL in 1 CANISTER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/06/2010 Labeler - Global Marketing Resources, Inc. (965102788)
