Label: AZURO- alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 49955-100-10, 49955-100-13, 49955-100-25, 49955-100-50, view more49955-100-60 - Packager: Noveko 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 January 4, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- STOP USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- GENERAL PRECAUTIONS
- INACTIVE INGREDIENT
- QUESTIONS
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL
ANTISEPTIC HAND SANITIZER
AZURO
ORIGINAL
SCENTED GEL
KILLS 99.9% OF COMMON BACTERIA OR GERMS!
70% V/V Ethyl Alcohol
formula enriched with
Vitamin E and Aloe vera.
Simple and convenient,
Azuro sanitizes without
the use of water.
Emollients leave hands
feeling soft and smooth
even during prolonged use.
fl oz. ( L/mL)
-
INGREDIENTS AND APPEARANCE
AZURO
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49955-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 L in 1 L Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49955-100-10 1 L in 1 BOTTLE 2 NDC:49955-100-13 1.3 L in 1 BOTTLE 3 NDC:49955-100-50 0.5 L in 1 BOTTLE 4 NDC:49955-100-25 0.25 L in 1 BOTTLE 5 NDC:49955-100-60 0.06 L in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 11/18/2009 Labeler - Noveko Inc (205614519)