Label: MEDICHOICE HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 55504-4000-1 - Packager: Donovan Industries, 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 December 10, 2009
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
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WARNINGS
Warnings:
Flammable. Keep away from heat or flame.
For external use only.
Do not use in the eyes.
In case of deep or puncture wounds, consult doctor.
In rare instances of irritation, discontinue use if irritation and redness develop.
If condition persists for more than 72 hours, consult a physician.
If swallowed, contact a physician or poison center.
Keep out of reach of children.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDICHOICE HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55504-4000 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) ISOPROPYL ALCOHOL (UNII: ND2M416302) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) ETHYLENEDIAMINE (UNII: 60V9STC53F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55504-4000-1 118 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 12/31/2009 Labeler - Donovan Industries, Inc. (096662267) Establishment Name Address ID/FEI Business Operations Chester Packaging, LLC. Inc. 004237806 manufacture