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SunDrops 73 - 63621-355-50 - (Alcohol)

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Drug Information of SunDrops 73

Product NDC: 63621-355
Proprietary Name: SunDrops 73
Non Proprietary Name: Alcohol
Active Ingredient(s): .65    mL/mL & nbsp;   Alcohol
Administration Route(s): CUTANEOUS
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of SunDrops 73

Product NDC: 63621-355
Labeler Name: Sunburst Chemicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED OTHER
Start Marketing Date: 20091014

Package Information of SunDrops 73

Package NDC: 63621-355-50
Package Description: 500 mL in 1 BOTTLE, PUMP (63621-355-50)

NDC Information of SunDrops 73

NDC Code 63621-355-50
Proprietary Name SunDrops 73
Package Description 500 mL in 1 BOTTLE, PUMP (63621-355-50)
Product NDC 63621-355
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Alcohol
Dosage Form Name LIQUID
Route Name CUTANEOUS
Start Marketing Date 20091014
Marketing Category Name UNAPPROVED OTHER
Labeler Name Sunburst Chemicals, Inc.
Substance Name ALCOHOL
Strength Number .65
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of SunDrops 73


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