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Mellow Instant Hand Sanitizer Original - 50154-0040-7 - (Ethyl Alcohol)

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Drug Information of Mellow Instant Hand Sanitizer Original

Product NDC: 50154-0040
Proprietary Name: Mellow Instant Hand Sanitizer Original
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 62    mL/100mL & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Mellow Instant Hand Sanitizer Original

Product NDC: 50154-0040
Labeler Name: Lantern Enterprises Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20091230

Package Information of Mellow Instant Hand Sanitizer Original

Package NDC: 50154-0040-7
Package Description: 236 mL in 1 BOTTLE (50154-0040-7)

NDC Information of Mellow Instant Hand Sanitizer Original

NDC Code 50154-0040-7
Proprietary Name Mellow Instant Hand Sanitizer Original
Package Description 236 mL in 1 BOTTLE (50154-0040-7)
Product NDC 50154-0040
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20091230
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Lantern Enterprises Ltd.
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Mellow Instant Hand Sanitizer Original


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