Acetaminophen
- Product NDC
- 68071-5239
- Requested package NDC
- 68071-5239-3
- 11-digit product format
- 680715239
- Labeler code
- 68071
- Product ID
- 68071-5239_2a95afd1-cd26-371c-e063-6294a90a97d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Extra Strength Pain Relief
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1989-01-01
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acetaminophen
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 198440 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| a32f346e-71d0-cc11-e053-2a95a90ae88c | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68071-5239-9 | 2022-02-07 | C162847 | 48780-1 | d6a99b39-bd7b-a426-e053-dadaa90af4c2 | gc201 |
| 68071-5239-9 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-bd7b-a426-e053-dadaa90af4c2 | gc201 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-5239-3 | Acetaminophen | 30 in 1 BOTTLE | TABLET | 30 | 7 | |
| 68071-5239-5 | Acetaminophen | 45 in 1 BOTTLE | TABLET | 45 | 7 | |
| 68071-5239-9 | Acetaminophen | 90 in 1 BOTTLE | TABLET | 90 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-5239 | ACETAMINOPHEN (EXTRA STRENGTH PAIN RELIEF) TABLET [NUCARE PHARMACEUTICALS,INC.] | 7 | Current NDC, Legacy NDC, 3 package rows | 20250101_a32f346e-71d0-cc11-e053-2a95a90ae88c.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 |
|---|---|---|---|---|---|---|
| SENOKOT | STANDARDIZED SENNA | A-S Medication Solutions | 0c6e6bdd-9f49-4550-b60a-8f58b7c0f090 | 2026-09-09 | Warnings | M007 |
| Bisacodyl | BISACODYL | KROGER COMPANY | a13a8eec-3652-8c57-e053-2995a90aaebf | 2026-09-09 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | TARGET Corporation | 4180a35b-cc50-46ae-a100-99bb218c10ff | 2026-09-09 | Warnings | M007 |
| fiber laxative | PSYLLIUM HUSK | Raritan Pharmaceuticals Inc | 22e927bd-5734-424e-8870-1aaa18f1265e | 2026-09-08 | Warnings | M007 |
| DRx Choice Fiber Therapy | METHYLCELLULOSE | RARITAN PHARMACEUTICALS INC | 5e5749f7-074e-4bbc-9f33-5090e603fdb4 | 2026-09-08 | Warnings | M007 |
| Bisacodyl Stimulant Laxative | BISACODYL | Raritan Pharmaceuticals Inc | b99c1a6d-3034-4822-8540-210179c06857 | 2026-09-08 | Warnings | M007 |
| Daily Fiber Sugar Free | PSYLLIUM HUSK | Raritan Pharmaceuticals Inc | 9c4c41d8-a2d5-4168-9e97-9f9d47fc5e63 | 2026-09-08 | Warnings | M007 |
| DRx Choice Fiber Therapy | METHYLCELLULOSE | RARITAN PHARMACEUTICALS INC | 56c7f197-f01a-4611-a761-cda18da6eed0 | 2026-09-08 | Warnings | M007 |
| Sennosides 8.6 mg | SENNOSIDES | Morepen Bio Inc | 562c9f11-0ba1-011d-e063-6394a90a604a | 2026-09-05 | Warnings | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Target Corporation | 87f98e6c-a3a1-4ca5-bd56-977e38f48914 | 2026-09-04 | Warnings, Adverse reactions | M007 |
| Kroger Stool Softener Fruit Punch | DOCUSATE SODIUM | KROGER COMPANY | b86f8f3d-594e-466c-854a-b8bff9f7a0b8 | 2026-09-02 | Warnings | M007 |
| Oil | MINERAL OIL | Atlantic Biologicals Corp. | 5a82197b-281d-76c0-e063-6294a90a5746 | 2026-09-02 | Warnings, Adverse reactions | M007 |
| Kroger Senna Laxative Regular Strength | SENNOSIDES | KROGER COMPANY | dbb040bb-21f9-43e8-9705-689aeee4d04c | 2026-09-01 | Warnings | M007 |
| OneLAX SENNA | SENNA | Akron Pharma Inc. | 27fa8f54-ed84-4afd-8da3-8754da48643b | 2026-09-01 | Warnings | M007 |
| OneLAX Saline Laxative | MAGNESIUM CITRATE | AKRON PHARMA INC | 44c87bbc-2507-4b87-a74b-02f4acb30cf4 | 2026-09-01 | Warnings | M007 |
| OneLAX Saline Laxative | MAGNESIUM CITRATE | AKRON PHARMA INC | e6de00e6-dd81-4aab-af23-04fab261c6ff | 2026-09-01 | Warnings | M007 |
| EZ2Go Magnesium Citrate Saline Laxative Lemon Flavor | MAGNESIUM CITRATE | Valley Medical Products LLC | 5a71e88c-d8cc-a8bb-e063-6294a90af4f7 | 2026-09-01 | Warnings | M007 |
| Fiber Caplets | CALCIUM POLYCARBOPHIL | THE KROGER CO. | d6856f59-ccc3-40fc-9bf1-7a5394ed12da | 2026-09-01 | Warnings | M007 |
| Mineral Oil | MINERAL OIL | Your Military Exchanges | 6025dce6-02e8-418c-a248-0b5c33ff6067 | 2026-08-28 | Warnings, Adverse reactions | M007 |
| Magnesium Citrate | MAGNESIUM CITRATE | Chain Drug Marketing Association | 583b64e7-e48d-6ba6-e063-6294a90ad4d7 | 2026-08-28 | Warnings, Adverse reactions | M007 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198440 | acetaminophen 500 MG Oral Tablet | PSN | a32f346e-71d0-cc11-e053-2a95a90ae88c | 7 |
| 198440 | acetaminophen 500 MG Oral Tablet | SCD | a32f346e-71d0-cc11-e053-2a95a90ae88c | 7 |
| 198440 | APAP 500 MG Oral Tablet | SY | a32f346e-71d0-cc11-e053-2a95a90ae88c | 7 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 68071-5239-3 | 68071523903 | 30 TABLET in 1 BOTTLE (68071-5239-3) | 30 tablet | 2020-04-13 | No | No | Current |