NDC 70677-1152-01 - Nasal Decongestant PE 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
- 70677-1152
- Requested NDC
- 70677-1152-01
- Package NDCs from labels
- 70677-1152-1, 70677-1152-2, 70677-1152-01
- Manufacturer
- Strategic Sourcing Services LLC | LNK International, Inc.
- Effective date
- 2026-04-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Foster and Thrive 44-453 | Strategic Sourcing Services LLC | LNK International, Inc. | 2026-04-08 | HUMAN OTC DRUG LABEL |
| Phenylephrine HCl - Sportpharm LLC | ASCLEMED USA INC. DBA ENOVACHEM | Sportpharm LLC | ASCLEMED USA INC. DBA ENOVACHEM | 2026-03-06 | HUMAN OTC DRUG LABEL |
| NASAL DECONGESTANT PE - A-S Medication Solutions | A-S Medication Solutions | 2024-11-13 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70677-1152-1 | Nasal Decongestant PEMaximum Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 7 | |
| 70677-1152-1 | Nasal Decongestant PEMaximum Strength | 18 in 1 BLISTER PACK | TABLET, FILM COATED | 18 | 7 | |
| 70677-1152-2 | Nasal Decongestant PEMaximum Strength | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 7 | |
| 70677-1152-2 | Nasal Decongestant PEMaximum Strength | 18 in 1 BLISTER PACK | TABLET, FILM COATED | 18 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70677-1152 | NASAL DECONGESTANT PE MAXIMUM STRENGTH (PHENYLEPHRINE HCL) TABLET, FILM COATED [STRATEGIC SOURCING SERVICES LLC] | 6 | Current NDC, 4 package rows | 20250428_8460d4f9-8d7b-4ae4-8047-c2010d9c8013.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70677-1152-1 | EA - Each | 70677-1152 | 7db53ae9-73e8-4349-91d8-5d28fd49616d | 1 | 2023-09-05 |
| 70677-1152-2 | EA - Each | 70677-1152 | 9866d1bb-b8bc-4c68-8c2b-dd5a4c8acf81 | 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 |
|---|---|---|---|---|---|---|
| Daytime Cold and Flu Maximum Strength | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | 67849e09-2056-4013-98b1-d003ed3250a2 | 2026-08-31 | Warnings | M012 04JA59TNSJ |
| MAX Tussin Mucus and Chest Congestion Sugar Free | GUAIFENESIN | Akron Pharma Inc. | 3b023b91-e703-4599-9864-96d8c328b45c | 2026-08-31 | Warnings | M012 |
| MAX Tussin Mucus and Chest Congestion | GUAIFENESIN | Akron Pharma Inc. | ac874a31-5556-4669-937f-dcb52aaecd8a | 2026-08-31 | Warnings | M012 |
| MAX Tussin Cough and Chest Congestion DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Akron Pharma Inc. | e0ce4287-bfa1-4413-97c8-4fe2e39bda36 | 2026-08-31 | Warnings | M012 |
| Acetaminophen PM Extra Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | United Natural Foods, Inc. dba UNFI | 24173e77-92ec-4a87-a471-d6867837c180 | 2026-08-31 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | DOLGENCORP, LLC | 69af44c2-390c-4223-889a-d5555aef5778 | 2026-08-28 | Warnings | M012 |
| Tussin DM Daytime | DEXTROMETHORPHAN HBR, GUAIFENESIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 432d4833-2eaf-4f7c-b6b4-41043a6b7e2a | 2026-08-28 | Warnings | M012 |
| Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Your Military Exchanges | 13fcc43c-bdda-4b65-b6d7-23b39e683651 | 2026-08-28 | Warnings, Adverse reactions | M012 |
| Multi-Symptom Allergy | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL | Walgreen Company | 5170c450-989d-44fa-ab38-86c78feae3b6 | 2026-08-28 | Warnings | M012 04JA59TNSJ |
| REFRESH LIQUIGEL | CARBOXYMETHYLCELLULOSE SODIUM | Allergan, Inc. | 4b8b2f6a-4b89-446c-9e5b-9b83c453a01d | 2026-08-28 | Warnings | K679OBS311 |
| Pain Reliever PM Extra strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Walgreens | 54cbbc5f-908b-47b2-b37f-3646354d3568 | 2026-08-27 | Warnings | M012 |
| Maximum Strength Mucus Relief | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Hyvee Inc | 4e578c7a-88d4-e4cd-e063-6394a90aac44 | 2026-08-27 | Warnings | M012 04JA59TNSJ |
| MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50 | SUNSCREEN SPF50 | Guangzhou Meixi Biotechnology Co., Ltd. | 5a0b4bd2-f6ad-35dc-e063-6294a90a8a66 | 2026-08-27 | Warnings | 15FIX9V2JP |
| MUCUS RELIEF | GUAIFENESIN | Geri-Care Pharmaceuticals, Corp | 5afb242f-fac9-dc81-e063-6394a90a8448 | 2026-08-27 | Warnings | M012 |
| daytime cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE | Amazon.com Services LLC | 6de619d3-0ab0-43e7-8dac-7bbd5368ac65 | 2026-08-27 | Warnings | M012 |
| Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu Maximum Strength | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, ACETAMINOPHEN, DIPHENHYDRAMINE HCI | Walgreens | 366ddac8-9e8a-41bd-a7f7-48213485a5f8 | 2026-08-27 | Warnings | M012 |
| Nighttime Cold and Flu Maximum Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI | Walgreens | 37896933-3ed3-457f-8a32-ee0d784a19e8 | 2026-08-27 | Warnings | M012 04JA59TNSJ |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Amazon.com Services LLC | 298e9164-e378-4b39-a944-bfc8f8baa4de | 2026-08-27 | Warnings | M012 |
| DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum Strength | DAYTIME ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, NIGHTTIME ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI | Walgreens | 3b4b3b04-eff9-4e06-8b37-f6729671d07f | 2026-08-27 | Warnings | M012 |
| MELAO Hydrating Lightweight Sunscreen | AVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDE | Guangdong Aimu Biological Technology Co., Ltd | 59eeaea1-d726-99f3-e063-6394a90aeea3 | 2026-08-26 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.