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NDC 00126-0016-61 PreviDent 6.1 mg/mL Details

PreviDent 6.1 mg/mL

PreviDent is a DENTAL GEL, DENTIFRICE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Colgate Oral Pharmaceuticals, Inc.. The primary component is SODIUM FLUORIDE.

MedlinePlus Drug Summary

Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 00126-0016-61
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Fluoride

Product Information

NDC	00126-0016
Product ID	0126-0016_f4c2f476-bdd5-49d1-80f7-361be61e47e5
Associated GPIs	88402020004020
GCN Sequence Number	060583
GCN Sequence Number Description	fluoride (sodium) PASTE (ML) 1.1 % DENTAL
HIC3	D2A
HIC3 Description	FLUORIDE PREPARATIONS
GCN	26755
HICL Sequence Number	001127
HICL Sequence Number Description	FLUORIDE (SODIUM)
Brand/Generic	Brand
Proprietary Name	PreviDent
Proprietary Name Suffix	5000 Dry Mouth
Non-Proprietary Name	Sodium fluoride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	GEL, DENTIFRICE
Route	DENTAL
Active Ingredient Strength	6.1
Active Ingredient Units	mg/mL
Substance Name	SODIUM FLUORIDE
Labeler Name	Colgate Oral Pharmaceuticals, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED DRUG OTHER
Application Number	n/a
Listing Certified Through	2024-12-31

Package

NDC 00126-0016-61 (00126001661)

Pricing Information	N/A
NDC Package Code	0126-0016-61
Billing NDC	00126001661
Package	100 mL in 1 BOTTLE (0126-0016-61)
Marketing Start Date	2009-07-06
NDC Exclude Flag	N