NDC 70677-1017-01 - Nasal Decongestant Maximum Strength
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
- 70677-1017
- Requested NDC
- 70677-1017-01
- Package NDCs from labels
- 70677-1017-1, 70677-1017-2, 70677-1017-3, 70677-1017-01
- Manufacturer
- Strategic Sourcing Services LLC | LNK International, Inc.
- Effective date
- 2026-09-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Foster and Thrive 44-112 | Strategic Sourcing Services LLC | LNK International, Inc. | 2026-09-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70677-1017-1 | Nasal DecongestantMaximum Strength | 24 in 1 BLISTER PACK | TABLET, FILM COATED | 24 | 5 | |
| 70677-1017-1 | Nasal DecongestantMaximum Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 5 | |
| 70677-1017-2 | Nasal DecongestantMaximum Strength | 24 in 1 BLISTER PACK | TABLET, FILM COATED | 24 | 5 | |
| 70677-1017-2 | Nasal DecongestantMaximum Strength | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 5 | |
| 70677-1017-3 | Nasal DecongestantMaximum Strength | 24 in 1 BLISTER PACK | TABLET, FILM COATED | 24 | 5 | |
| 70677-1017-3 | Nasal DecongestantMaximum Strength | 4 in 1 CARTON | TABLET, FILM COATED | 4 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70677-1017 | NASAL DECONGESTANT MAXIMUM STRENGTH (PSEUDOEPHEDRINE HCL) TABLET, FILM COATED [STRATEGIC SOURCING SERVICES LLC] | 4 | Current NDC, 6 package rows | 20250410_f6742552-1cdf-497f-9849-436c90b99a08.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70677-1017-1 | EA - Each | 70677-1017 | b399867a-5077-43db-83f4-0aee0e4fafac | 1 | 2023-09-05 |
| 70677-1017-2 | EA - Each | 70677-1017 | 4e1cff48-b1fe-4e25-977c-4233d7077b01 | 1 | 2023-09-05 |
| 70677-1017-3 | EA - Each | 70677-1017 | 02bb30e1-c830-4db6-b107-9716e4157d00 | 1 | 2023-09-05 |
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 |
|---|---|---|---|---|---|---|
| Guaifenesin | GUAIFENESIN | Method Pharmaceuticals, LLC | 1539c3d4-d982-7d4e-e063-6394a90ad7d6 | 2025-10-21 | Warnings | M012 |
| Guaifenesin | GUAIFENESIN | Method Pharmaceuticals, LLC | 312ce620-4841-7488-e054-00144ff88e88 | 2025-10-21 | Warnings | M012 |
| M-Dryl | DIPHENHYDRAMINE HYDROCHLORIDE | Method Pharmaceuticals, LLC | 5a60c923-8bb7-427f-9636-08ed5474f71b | 2025-10-21 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | ARMY AND AIR FORCE EXCHANGE SERVICE | 97ed70a0-b692-4c12-90d6-72b3c87e554c | 2025-10-21 | Warnings | M012 |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | United Natural Foods, Inc. dba UNFI | 311e2b6b-21cb-4b4c-a78d-a0732d29602f | 2025-10-21 | Warnings | M012 |
| Daytime Nighttime Cold Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | United Natural Foods, Inc. dba UNFI | 13910ea1-37dd-43bb-9fe8-e843f59201b7 | 2025-10-21 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | Amerisource Bergen | d6f185b6-8538-4eac-98da-83760c34b488 | 2025-10-20 | Warnings | M012 |
| Quantum Health Bing Cherry Flavor | MENTHOL, UNSPECIFIED FORM | Quantum, Inc. | 94d40c95-fa2b-42cf-b9f5-a5027d86401d | 2025-10-20 | Warnings | M012 |
| Quantum Health Meyer Lemon and Honey Flavor | MENTHOL, UNSPECIFIED FORM | Quantum, Inc. | fe780067-5a20-4d55-a108-91237cd9e5f4 | 2025-10-20 | Warnings | M012 |
| Clinical Skin Filter Tinted Sunscreen | CLINICAL SKIN FILTER TINTED SUNSCREEN | KRX RESOURCES SDN. BHD. | 22b8856b-671f-def3-e063-6394a90a4ea0 | 2025-10-18 | Warnings | 15FIX9V2JP |
| Clinical Skin Filter Tinted Sunscreen Medium Dark | CLINICAL SKIN FILTER TINTED SUNSCREEN MEDIUM DARK | KRX RESOURCES SDN. BHD. | 22cead37-f862-e859-e063-6394a90a86ce | 2025-10-18 | Warnings | 15FIX9V2JP |
| Krx Aesthetics All Day Glow Sunblocker | KRX AESTHETICS ALL DAY GLOW SUNBLOCKER | KRX RESOURCES SDN. BHD. | 22a60fb9-0fea-92c0-e063-6394a90a088c | 2025-10-18 | Warnings | 15FIX9V2JP |
| OneSsip Diphenhydramine HCl 12.5 mg/ 5 mL Oral Solution (Cherry) | DIPHENHYDRAMINE HCL | MEDWISE LIFESCIENCES INC. | 4157e680-37ac-eb4c-e063-6394a90a2a99 | 2025-10-17 | Warnings | M012 |
| Norel AD | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND PHENYLEPHRINE HCL | U.S. PHARMACEUTICAL CORPORATION | 53d9ed3c-212d-4b12-ac35-8bd49382b49d | 2025-10-17 | Warnings | M012 |
| Severe Congestion, Cough, Cold and Flu Relief Maximum Strength, Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, TRIPROLIDINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 92c570ff-139f-49ff-a7bd-8a540ecc07c7 | 2025-10-17 | Warnings | M012 |
| NoHist DM | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE AND PHENYLEPHRINE HYDROCHLORIDE | Larken Laboratories, Inc. | 6aafe912-28ff-442f-8e07-b3c5993ac943 | 2025-10-16 | Warnings | M012 |
| DD Cream | DD CREAM | DERMAdoctor, Inc. | 08c9a0cf-ee78-483b-e054-00144ff88e88 | 2025-10-16 | Warnings | 15FIX9V2JP |
| Signature Care Original | OXYMETAZOLINE HYDROCHLORIDE | SAFEWAY, INC. | f7ad687b-dcaf-928c-e053-6294a90a6abe | 2025-10-16 | Warnings | M012 |
| Daytime Nighttime Cold Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Care One (Retail Business Services, LLC.) | 90ccb29c-9967-46cb-a409-e440344e1a1a | 2025-10-15 | Warnings | M012 |
| Ciele Filter and Protect | TITANIUM DIOXIDE, ZINC OXIDE | Ciele | 0309b0ef-baca-b41d-e063-6294a90a49d7 | 2025-10-15 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.