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Morning Fresh - 67777-171-02 - (Sodium Monofluorophosphate)

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Drug Information of Morning Fresh

Product NDC: 67777-171
Proprietary Name: Morning Fresh
Non Proprietary Name: Sodium Monofluorophosphate
Active Ingredient(s): 1    mg/g & nbsp;   Sodium Monofluorophosphate
Administration Route(s): ORAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of Morning Fresh

Product NDC: 67777-171
Labeler Name: Dynarex Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100608

Package Information of Morning Fresh

Package NDC: 67777-171-02
Package Description: 78 g in 1 TUBE (67777-171-02)

NDC Information of Morning Fresh

NDC Code 67777-171-02
Proprietary Name Morning Fresh
Package Description 78 g in 1 TUBE (67777-171-02)
Product NDC 67777-171
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Monofluorophosphate
Dosage Form Name PASTE
Route Name ORAL
Start Marketing Date 20100608
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dynarex Corporation
Substance Name SODIUM MONOFLUOROPHOSPHATE
Strength Number 1
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Morning Fresh


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