NDC 17856-0353-2 - Pharbetol Regular 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
- 17856-0353
- Requested NDC
- 17856-0353-2
- Package NDCs from labels
- 17856-0353-2, 17856-0353-1, 17856-0353-4, 17856-0353-3
- Manufacturer
- ATLANTIC BIOLOGICALS CORP.
- Effective date
- 2025-06-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PHARBEST IBUPROFEN Drug Facts | ATLANTIC BIOLOGICALS CORP. | 2025-06-05 | HUMAN OTC DRUG LABEL |
| Pharbetol Regular strength - ATLANTIC BIOLOGICALS CORP. | UNIT DOSE SOLUTIONS | ATLANTIC BIOLOGICALS CORP. | UNIT DOSE SOLUTIONS | 2024-04-30 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 17856-0353-1 | 2024-06-26 | C162847 | 48780-1 | 1030e365-250f-111a-e063-dadaa90a10e2 | PHARBEST IBUPROFEN Drug Facts |
| 17856-0353-1 | 2024-01-30 | C162847 | 48780-1 | 1030e365-250f-111a-e063-dadaa90a10e2 | PHARBEST IBUPROFEN Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-0353-1 | PharbetolRegular strength | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | 3 | |
| 17856-0353-2 | PharbetolRegular strength | 1 in 1 POUCH | TABLET | 1 | 3 | |
| 17856-0353-4 | PharbetolRegular strength | 24 in 1 BOTTLE | TABLET | 24 | 3 | |
| 17856-0353-3 | PharbetolRegular strength | 28 in 1 BOTTLE | TABLET | 28 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-0353 | PHARBETOL REGULAR STRENGTH (ACETAMINOPHEN) TABLET [ATLANTIC BIOLOGICALS CORP.] | 2 | Current NDC, Legacy NDC, 3 package rows | 20240627_05a91d24-b498-4ba2-a275-68b871cf62d2.zip |
| 17856-0353 | PHARBETOL REGULAR STRENGTH (ACETAMINOPHEN) TABLET [ATLANTIC BIOLOGICALS CORP.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20240508_bd26081c-e81e-42e8-b3da-2813863a51df.zip |
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 |
|---|---|---|---|---|---|---|
| Maximum Strength Nighttime Cold and Flu | ACETAMINOPHEN , DIPHENHYDRAMINE HCL,PHENYLEPHRINE HCL | THE KROGER CO | 058b2021-8a61-40b0-8a2e-a784d2b847fb | 2026-09-02 | Warnings | 362O9ITL9D |
| Daytime Cold and Flu Relief | ACETAMINOHPEN, DEXTROMETHORPHAN HBR, GUAIFENESIN PHENYLEPHRINE HCL | The Kroger Co. | 494e69ef-dc9f-4e14-b856-5eaf0f541a03 | 2026-09-02 | Warnings | 362O9ITL9D |
| Adult Low Dose Chewable Aspirin | ASPIRIN | Farmacias De Similares TX LLC | 513ea306-74c6-96e3-e063-6394a90a8262 | 2026-09-01 | Warnings | M013 |
| Kroger Children Pain plus Fever chewables | ACETAMINOPHEN | KROGER COMPANY | 83b5733c-70a1-4383-9729-2eb896d0149a | 2026-09-01 | Warnings | M013 362O9ITL9D |
| Pain Reliever PM Extra Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | TOP CARE (Topco Associates LLC) | 923b443d-73cc-4c52-92e4-a075786b1ae3 | 2026-09-01 | Warnings | M013 362O9ITL9D |
| ACETAMINOPHEN PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Amazon.com Services LLC | 99a137d6-07eb-43bc-b4b4-1a23041d595e | 2026-08-31 | Warnings | M013 362O9ITL9D |
| Acetaminophen Extra Strength | ACETAMINOPHEN | CVS PHARMACY | 64a1ebe7-af28-4b09-96e8-28fa4dcc52bd | 2026-08-31 | Warnings | M013 362O9ITL9D |
| Daytime Cold and Flu Multi Symptom Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | e85b4c2a-d4e0-452c-9a08-fcc0ff6eaa21 | 2026-08-31 | Warnings | 362O9ITL9D |
| MAX relief junior Grape | CHILDRENS ACETAMINOPHEN | Akron Pharma Inc. | cc769c26-556a-4831-bd75-61a7383aa707 | 2026-08-31 | Warnings | M013 362O9ITL9D |
| MAX relief junior | CHILDRENS ACETAMINOPHEN | Akron Pharma Inc. | ebb3b4ba-2d0b-48d9-b6ee-6d4696aea047 | 2026-08-31 | Warnings | M013 362O9ITL9D |
| Daytime Cold and Flu Maximum Strength | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | 67849e09-2056-4013-98b1-d003ed3250a2 | 2026-08-31 | Warnings | 362O9ITL9D |
| MAX relief junior | ACETAMINOPHEN | Akron Pharma Inc. | 0e43b885-3843-4f11-9a53-02a38c228313 | 2026-08-31 | Warnings | M013 362O9ITL9D |
| MAX relief junior | CHILDREN ACETAMINOPHEN | Akron Pharma Inc. | d7874e4d-0b38-4bb1-9a62-aa4f66d9baf9 | 2026-08-31 | Warnings | M013 362O9ITL9D |
| MAX relief junior Grape | CHILDREN ACETAMINOPHEN | Akron Pharma Inc. | 3c7a7f40-4963-4fd1-942e-93fa08a45830 | 2026-08-31 | Warnings | M013 362O9ITL9D |
| Genexa Kids Pain and Fever | ACETAMINOPHEN | Genexa Inc. | 5a615118-33c9-1520-e063-6394a90a21a6 | 2026-08-31 | Warnings | M013 362O9ITL9D |
| Acetaminophen PM Extra Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | United Natural Foods, Inc. dba UNFI | 24173e77-92ec-4a87-a471-d6867837c180 | 2026-08-31 | Warnings | 362O9ITL9D |
| acetaminophen extra strength | ACETAMINOPHEN | Sam's West Inc | dd99efd0-4ca4-4dc6-a940-bebd17ac8f8d | 2026-08-28 | Warnings | M013 362O9ITL9D |
| Aspirin 81 mg | ASPIRIN | HAWAII REPACK, INC. | ac94cce3-9a39-41de-bb8b-10a5e5b8e83b | 2026-08-28 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | REMEDYREPACK INC. | 464e404a-1957-44a2-a53a-f2a9d3c15bde | 2026-08-28 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Multi-Symptom Allergy | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL | Walgreen Company | 5170c450-989d-44fa-ab38-86c78feae3b6 | 2026-08-28 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.