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Mentholatum Natural Ice - 10742-3004-1 - (dimethicone, octinoxate, octisalate)

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Drug Information of Mentholatum Natural Ice

Product NDC: 10742-3004
Proprietary Name: Mentholatum Natural Ice
Non Proprietary Name: dimethicone, octinoxate, octisalate
Active Ingredient(s): 10; 75; 50    mg/g; mg/g; mg/g & nbsp;   dimethicone, octinoxate, octisalate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Mentholatum Natural Ice

Product NDC: 10742-3004
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19990119

Package Information of Mentholatum Natural Ice

Package NDC: 10742-3004-1
Package Description: 1 TUBE in 1 BLISTER PACK (10742-3004-1) > 4.5 g in 1 TUBE

NDC Information of Mentholatum Natural Ice

NDC Code 10742-3004-1
Proprietary Name Mentholatum Natural Ice
Package Description 1 TUBE in 1 BLISTER PACK (10742-3004-1) > 4.5 g in 1 TUBE
Product NDC 10742-3004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dimethicone, octinoxate, octisalate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19990119
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Mentholatum Company
Substance Name DIMETHICONE; OCTINOXATE; OCTISALATE
Strength Number 10; 75; 50
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of Mentholatum Natural Ice


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