Label: LIVE BETTER- benzalkonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 48871-003-01 - Packager: Health-Tech, Inc.
- 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 May 25, 2010
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- Official Label (Printer Friendly)
- Active Ingredient
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Other information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LIVE BETTER HAND SANITIZER
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48871-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride .0013 mL in 1 mL Inactive Ingredients Ingredient Name Strength Cetrimonium Chloride (UNII: UC9PE95IBP) Edetate disodium (UNII: 7FLD91C86K) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48871-003-01 6 in 1 CASE 1 12 in 1 CARTON 1 2 in 1 BLISTER PACK 1 7.5 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 03/31/2010 Labeler - Health-Tech, Inc. (084007889) Establishment Name Address ID/FEI Business Operations Health-Tech, Inc. 084007889 manufacture