Label: ANDYS- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73755-110-01 - Packager: Brand Name Distributors
- 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 March 29, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- DIRECTIONS AND USD
- INACTIVE INGREDIENTS
- WARNING
- Keep Out of Reach of Children.
- PURPOSE
- DOSAGE
- ANDY's HAND SANITIZER Unscented
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INGREDIENTS AND APPEARANCE
ANDYS
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73755-110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER O-18 (UNII: 7QV8F8BYNJ) 1 mL in 1 mL TROLAMINE (UNII: 9O3K93S3TK) 1 mL in 1 mL CARBOMER 1342 (UNII: 809Y72KV36) 1 mL in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73755-110-01 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/21/2020 Labeler - Brand Name Distributors (078570365)