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 |
|---|---|---|---|---|---|---|
| Mucinex D | GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE | Reckitt Benckiser LLC | d5f046c0-66b9-4cdc-9a1e-8e2cb5ece84f | 2026-05-27 | Warnings | 6V9V2RYJ8N |
| Goodmeds Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Cabinet Health P.B.C. | 37533188-8c91-428b-a796-c5afd9e4959f | 2026-05-27 | Warnings | M012 |
| Delsym Cough Plus Chest Congestion DM | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | Reckitt Benckiser LLC | 8252cdec-b668-4450-b045-e093479ab542 | 2026-05-27 | Warnings | M012 |
| Delsym Nighttime Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND TRIPROLIDINE HYDROCHLORIDE | Reckitt Benckiser LLC | 27f9d2db-38ce-41d2-8f1a-0eb171600274 | 2026-05-27 | Warnings | M012 |
| Delsym Cough Plus Sore Throat | ACETAMINOPHEN AND DEXTROMETHORPHAN HYDROBROMIDE | Reckitt Benckiser LLC | b37b786e-0cce-419d-94ed-3b64a1eb1201 | 2026-05-27 | Warnings | M012 |
| Delsym Cough | DEXTROMETHORPHAN HYDROBROMIDE | Reckitt Benckiser LLC | a43d59f9-3a6c-4a7c-b98d-b86d6035f716 | 2026-05-27 | Warnings | M012 |
| Cold and Flu Relief Severe Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Rite Aid Corporation | 5700ef26-ffa6-480a-bf36-bd5111799e9b | 2026-05-27 | Warnings | M012 |
| Air Power | GUAIFENESIN | Schwabe North America, Inc | 5cdefc7a-6242-4681-88a3-04422a1d48d3 | 2026-05-27 | Warnings | M012 |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | WALMART INC. | adb658c8-db8d-4db6-80c8-e0f2de88a2de | 2026-05-27 | Warnings | M012 |
| Daytime Cold and Flu Non Drowsy | ACETAMINOHPEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | CVS Pharmacy | c71427d4-707f-411f-8bd4-133517a9992b | 2026-05-26 | Warnings | M012 |
| Leader Mucus Relief D | GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE | Cardinal Health 110, LLC. dba Leader | 12971fb2-2314-4443-bf70-b7eb5859b148 | 2026-05-26 | Warnings | 6V9V2RYJ8N |
| Daytime Cold and Flu | ACETAMINOPHEN DEXTROMETHORPHAN HBR PHENYLEPHRINE HCL | CVS PHARMACY, INC | 643e929d-9e62-4260-91ee-e88a184dd7cd | 2026-05-26 | Warnings | M012 |
| TopCare Day Time Nite Time Cold and Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Topco Associates LLC | c00ff684-acaf-4fbe-bc74-7e48751b927d | 2026-05-26 | Warnings | M012 |
| Goodmeds Non-Drowsy Nasal Decongestant PE | PHENYLEPHRINE | Cabinet Health P.B.C. | 4e75da23-35f2-431c-92cb-c2c4cb3f09f1 | 2026-05-26 | Warnings | M012 |
| O HUI DAY SHIELD PERFECT SUN BLACK BROAD SPECTRUM SPF 50 SUNSCREEN | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | LG H&H Co., Ltd. | 52ba9423-8b9b-38f7-e063-6394a90a95da | 2026-05-26 | Warnings | 15FIX9V2JP |
| Night Time Cold and Flu Relief Multi Symptom | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | CVS Pharmacy | 13492631-d5de-4562-a201-664f7d3591de | 2026-05-26 | Warnings | M012 |
| Sinufrin Decongestant | NASAL CONGESTION RELIEF | NeilMed Pharmaceuticals Inc | 52a2e5f9-e0a2-02f7-e063-6294a90a3ae9 | 2026-05-25 | Warnings | M012 |
| Cough Suppressant Adult | DEXTROMETHORPHAN HYDROBROMIDE | Rugby Laboratories | 47b713bd-4c1e-f44a-e063-6294a90a63d3 | 2026-05-25 | Warnings | M012 |
| ClorRelief | CHLORPHENIRAMINE MALEATE | FERRER MEDICAL INNOVATIONS LLC | db729011-f72f-5911-e053-2a95a90a68bf | 2026-05-22 | Warnings | M012 |
| Childrens Dye Free Allergy Relief | DIPHENHYDRAMINE HCL | Rite Aid Corporation | 74ff4f0d-7952-4b74-b1b2-5a2beab91f7c | 2026-05-22 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.