HEB - 37808-171-19 - (Fluoride)

Alphabetical Index


Drug Information of HEB

Product NDC: 37808-171
Proprietary Name: HEB
Non Proprietary Name: Fluoride
Active Ingredient(s): .454    g/100g & nbsp;   Fluoride
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of HEB

Product NDC: 37808-171
Labeler Name: HEB
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121201

Package Information of HEB

Package NDC: 37808-171-19
Package Description: 1 TUBE in 1 CARTON (37808-171-19) > 170 g in 1 TUBE (37808-171-12)

NDC Information of HEB

NDC Code 37808-171-19
Proprietary Name HEB
Package Description 1 TUBE in 1 CARTON (37808-171-19) > 170 g in 1 TUBE (37808-171-12)
Product NDC 37808-171
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20121201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HEB
Substance Name STANNOUS FLUORIDE
Strength Number .454
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of HEB


General Information