NDC 67659-080-01 - Up and UP Sensitive Toothpaste Enamel Strengthening formula
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
- 67659-080
- Requested NDC
- 67659-080-01
- Package NDCs from labels
- 67659-080-01, 67659-080-02
- Manufacturer
- Team Technologies, Inc
- Effective date
- 2010-08-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Potassium Nitrate and Sodium Fluoride - Team Technologies, Inc | Team Technologies, Inc | 2010-08-25 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 67659-080-02 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-c186-621f-e053-dbdaa90a74ad | UP and Up Sensitive Toothpaste Enamel Strengthening formula |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67659-080-01 | Up and UP Sensitive Toothpaste Enamel Strengthening formula | 113 g in 1 TUBE | PASTE | 113 | 1 | |
| 67659-080-02 | Up and UP Sensitive Toothpaste Enamel Strengthening formula | 1 in 1 CARTON | PASTE | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 67659-080 | UP AND UP SENSITIVE TOOTHPASTE ENAMEL STRENGTHENING FORMULA (POTASSIUM NITRATE AND SODIUM FLUORIDE) PASTE [TEAM TECHNOLOGIES, INC] | 1 | Legacy NDC, 2 package rows | 20100831_f1f1081f-c15d-4bcd-9372-830a822ab491.zip |
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SF 5000 Plus | 1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM | Cypress Pharmaceutical, Inc. | fa625ece-d873-491a-8d45-2833b64e5425 | 2016-07-01 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Meijer Kids Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distribution, Inc. | 7415511e-1ecf-4646-b64b-267fbf7d116b | 2016-06-02 | Warnings | 15FIX9V2JP |
| Meijer Baby Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distributing Inc. | 2434de23-bcc9-4a83-9945-16fc3f2b8c61 | 2016-06-01 | Warnings | 15FIX9V2JP |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 54c1a27c-5936-4ee2-a419-3891d3df9745 | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 RU45X2JN0Z |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 642fec99-c5c5-4ef2-986e-5b5f7cf460de | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 RU45X2JN0Z |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
| a82a82ab-ee33-4a07-8a3b-354c1394fd96 | f1f1081f-c15d-4bcd-9372-830a822ab491 | 2010-08-25 | Warnings | a82a82ab-ee33-4a07-8a3b-354c1394fd96 f1f1081f-c15d-4bcd-9372-830a822ab491 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.