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SunDrops 67 - 63621-353-80 - (Chloroxylenol)

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Drug Information of SunDrops 67

Product NDC: 63621-353
Proprietary Name: SunDrops 67
Non Proprietary Name: Chloroxylenol
Active Ingredient(s): .75    g/100mL & nbsp;   Chloroxylenol
Administration Route(s): CUTANEOUS
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of SunDrops 67

Product NDC: 63621-353
Labeler Name: Sunburst Chemicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100707

Package Information of SunDrops 67

Package NDC: 63621-353-80
Package Description: 500 mL in 1 BOTTLE, PUMP (63621-353-80)

NDC Information of SunDrops 67

NDC Code 63621-353-80
Proprietary Name SunDrops 67
Package Description 500 mL in 1 BOTTLE, PUMP (63621-353-80)
Product NDC 63621-353
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chloroxylenol
Dosage Form Name LIQUID
Route Name CUTANEOUS
Start Marketing Date 20100707
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Sunburst Chemicals, Inc.
Substance Name CHLOROXYLENOL
Strength Number .75
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of SunDrops 67


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