prevident 5000 dry mouth

Generic: sodium fluoride

Labeler: colgate oral pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name prevident 5000 dry mouth
Generic Name sodium fluoride
Labeler colgate oral pharmaceuticals, inc.
Dosage Form GEL, DENTIFRICE
Routes
DENTAL
Active Ingredients

sodium fluoride 6.1 mg/mL

Manufacturer
Colgate Oral Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0126-0016
Product ID 0126-0016_f4c2f476-bdd5-49d1-80f7-361be61e47e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2009-07-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01260016
Hyphenated Format 0126-0016

Supplemental Identifiers

RxCUI
392038 630194
UPC
0301260016610
UNII
8ZYQ1474W7

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name prevident 5000 dry mouth (source: ndc)
Generic Name sodium fluoride (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 6.1 mg/mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (0126-0016-61)
source: ndc

Packages (1)

0126-0016-61 100 mL in 1 BOTTLE (0126-0016-61)

Ingredients (1)

sodium fluoride (6.1 mg/mL)

Linked Drug Pages (1)

PreviDent 5000 Dry Mouth ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["DENTAL"], "spl_id": "f4c2f476-bdd5-49d1-80f7-361be61e47e5", "openfda": {"upc": ["0301260016610"], "unii": ["8ZYQ1474W7"], "rxcui": ["392038", "630194"], "spl_set_id": ["d93ee76f-454b-40bf-9357-39a2ae3b6ccb"], "manufacturer_name": ["Colgate Oral Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0126-0016-61)", "package_ndc": "0126-0016-61", "marketing_start_date": "20090706"}], "brand_name": "PreviDent 5000 Dry Mouth", "product_id": "0126-0016_f4c2f476-bdd5-49d1-80f7-361be61e47e5", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "0126-0016", "generic_name": "Sodium fluoride", "labeler_name": "Colgate Oral Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PreviDent", "brand_name_suffix": "5000 Dry Mouth", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": "6.1 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20090706", "listing_expiration_date": "20261231"}