Home NDC 68987-024 NDC 68987-024 - PureLife APF This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 68987-024
Package NDCs from labels 68987-024-12
Manufacturer PureLife Dental
Effective date 2014-05-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type PureLife APF - PureLife Dental PureLife Dental 2014-05-14 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68987-024-12 PureLife APF 125 g in 1 BOTTLE, PUMP AEROSOL, FOAM 125 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68987-024 PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 1 package rows 20140515_8eae4995-5905-4269-8d53-e7acb54856a3.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 HYDROFLUORIC ACID INACTIVE INGREDIENT RGL5YE86CZ PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 PHOSPHORIC ACID INACTIVE INGREDIENT E4GA8884NN PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 POLOXAMER 407 INACTIVE INGREDIENT TUF2IVW3M2 PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 SODIUM LAURETH-3 SULFATE INACTIVE INGREDIENT BPV390UAP0 PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 Water INACTIVE INGREDIENT 059QF0KO0R PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1 XYLITOL INACTIVE INGREDIENT VCQ006KQ1E PURELIFE APF (SODIUM FLUORIDE) AEROSOL, FOAM [PURELIFE DENTAL] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 35 of 78 · 1,541 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join PRO-SYS SODIUM FLUORIDE AND POTASSIUM NITRATE Benco Dental 4e470ba4-60bb-1815-e063-6294a90abacc 2025-12-01 Warnings Exact identifier unii: 8ZYQ1474W7 PRO-SYS SODIUM FLUORIDE Benco Dental 4e539cb2-bcbd-95fc-e063-6294a90a2121 2025-12-01 Warnings Exact identifier unii: 8ZYQ1474W7 PRO-SYS PROFESSIONAL SENSITIVITY, SLS FREE - MINT (5000 PPM) Benco Dental 4e4761d7-f1ab-aae4-e063-6294a90a214c 2025-12-01 Warnings Exact identifier unii: 8ZYQ1474W7 Cool sense Care Plus SODIUM FLUORIDE DONG IL PHARMS CO., LTD. 44763bf6-caf3-ec69-e063-6394a90a0ee1 2025-11-25 Warnings Exact identifier unii: 8ZYQ1474W7 DOCTRUST DOUBLEX Tooth SODIUM FLUORIDE DONG IL PHARMS CO.,LTD 44765e86-2eb2-6381-e063-6394a90a761f 2025-11-25 Warnings Exact identifier unii: 8ZYQ1474W7 DOCTRUST ONE S Tooth SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE DONG IL PHARMS CO.,LTD 4476923a-48f1-9f72-e063-6394a90a0708 2025-11-25 Warnings Exact identifier unii: 8ZYQ1474W7 TheraBreath for Kids Anticavity Wacky Watermelon SODIUM FLUORIDE Church & Dwight Co., Inc. 578f8010-6b1c-4c6b-91d3-e483ace40f66 2025-11-25 Warnings Exact identifier unii: 8ZYQ1474W7 PUR-WASH WATER Niagara Pharmaceuticals Inc. beda35c3-9a8b-47ad-e053-2995a90a7b1b 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R Easy Care First Aid Eyewash WATER Tender Corporation a070aac8-e6d2-ef10-e053-2a95a90aa5b1 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R PUR-WASH WATER Niagara Pharmaceuticals Inc. e07a064b-f680-405c-bbcd-24fac430951e 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R ULINE Eyewash EYEWASH Niagara Pharmaceuticals Inc. 2d7f22d2-320b-6af1-e063-6294a90addc6 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R Pur-Wash EYEWASH Niagara Pharmaceuticals, Inc. 0d43b1c1-2699-37f1-e054-00144ff88e88 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R PUR-WASH WATER Niagara Pharmaceuticals Inc. 777e1559-786f-8d54-e053-2991aa0aa98d 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R PUR-WASH WATER Niagara Pharmaceuticals Inc. 7289103a-5cbf-42f4-8848-e827149a43ca 2025-11-24 Warnings Exact identifier unii: 059QF0KO0R Sensodyne Cavity and Sensitivity POTASSIUM NITRATE, SODIUM FLUORIDE Haleon US Holdings LLC d002074b-0580-4247-b3c7-121b8c098697 2025-11-24 Warnings Exact identifier unii: 8ZYQ1474W7 HEB Extra Whitening FLUORIDE HEB 9bdcbd3f-095b-43d1-8a8e-0ba3eab14e0e 2025-11-21 Warnings Exact identifier unii: 8ZYQ1474W7 HEB Enamel Protection Multi Action POTASSIUM NITRATE, SODIUM FLUORIDE HEB 8255de83-aa60-b081-e053-2a91aa0afcdc 2025-11-21 Warnings Exact identifier unii: 8ZYQ1474W7 CVS Enamel Guard FLUORIDE CVS Pharmacy d9dfa515-426b-9059-e053-2a95a90a3885 2025-11-21 Warnings Exact identifier unii: 8ZYQ1474W7 CVS Pharmacy Enamel Guard FLUORIDE CVS Pharmacy 18295a1c-c2a6-489b-be34-9252b9e1e2b8 2025-11-21 Warnings Exact identifier unii: 8ZYQ1474W7 CVS Extra Whitening FLUORIDE CVS Pharmacy 3b019849-6585-4a8c-a90a-c7e9e617b3ef 2025-11-21 Warnings Exact identifier unii: 8ZYQ1474W7
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.