Package 0126-0016-61

Brand: prevident 5000 dry mouth

Generic: sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 0126-0016-61
Digits Only 0126001661
Product NDC 0126-0016
Product ID 0126-0016_f4c2f476-bdd5-49d1-80f7-361be61e47e5
Description

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

Marketing

Marketing Status
Marketed Since 2009-07-06
Brand prevident 5000 dry mouth
Generic sodium fluoride
Sample Package No

Linked Drug Pages (1)

PreviDent 5000 Dry Mouth ndc-match (0.95)

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"}