Label: LEMON SPLASH ANTI-BACTERIAL SCENTED HAND SANITIZER- alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 60533-006-29 - Packager: Best Accessory Group
- 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 August 13, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient:
- PURPOSE
- INDICATIONS & USAGE
- Warnings:
- WHEN USING
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- Inactive Ingredients:
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 29 mL Bottle Label
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INGREDIENTS AND APPEARANCE
LEMON SPLASH ANTI-BACTERIAL SCENTED HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60533-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) TROLAMINE (UNII: 9O3K93S3TK) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) ETHYL JOJOBATE (UNII: 2351QH8W1N) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60533-006-29 29 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/13/2013 Labeler - Best Accessory Group (078712219)