NOTTS - Extra Strength 500 mg
- Product NDC
- 82706-007
- 11-digit product format
- 827060007
- Labeler code
- 82706
- Product ID
- 82706-007_2df54d96-b18b-e9e3-e063-6294a90a6926
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- VIVUNT PHARMA LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-08-17
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 82706-007 | 82706-007-04 | D | Discontinued by firm | excluded / ndc_excluded.zip | ad56d346431e… | cc804d4bbf1e… | |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 82706-007 | 82706-007-04 | D | Discontinued by firm | excluded / ndc_excluded.zip | 367a005e9d99… | 383a685ebd0f… | |
| 2024-07-10 04:00 UTC · source 2024-07-09 | excluded package | package | 82706-007 | 82706-007-04 | D | Discontinued by firm | excluded / ndc_excluded.zip | 557ba5c1ecfa… | 9c80585c8c6e… |
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
- NOTTS - Extra Strength 500 mg
- 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 |
|---|---|
| e677f43d-b4ce-e5b0-e053-2a95a90ad67e | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82706-007-01 | NOTTS - Extra Strength 500 mg | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 82706-007-01 | NOTTS - Extra Strength 500 mg | 24 in 1 BOTTLE, PLASTIC | TABLET | 24 | 12 | |
| 82706-007-02 | NOTTS - Extra Strength 500 mg | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | 12 | |
| 82706-007-02 | NOTTS - Extra Strength 500 mg | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 82706-007-03 | NOTTS - Extra Strength 500 mg | 400 in 1 BOTTLE, PLASTIC | TABLET | 400 | 12 | |
| 82706-007-04 | NOTTS - Extra Strength 500 mg | 2 in 1 POUCH | TABLET | 2 | 12 | |
| 82706-007-04 | NOTTS - Extra Strength 500 mg | 3 in 1 CARTON | TABLET | 3 | 12 | |
| 82706-007-05 | NOTTS - Extra Strength 500 mg | 2 in 1 POUCH | TABLET | 2 | 12 | |
| 82706-007-05 | NOTTS - Extra Strength 500 mg | 50 in 1 CARTON | TABLET | 50 | 12 | |
| 82706-007-06 | NOTTS - Extra Strength 500 mg | 25 in 1 CARTON | TABLET | 25 | 12 | |
| 82706-007-06 | NOTTS - Extra Strength 500 mg | 25 in 1 BLISTER PACK | TABLET | 25 | 12 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Low Dose Aspiriun | ASPIRIN | AMERIFOODS TRADING COMPANY | 3802c96a-5e2a-ba9c-e063-6394a90abb78 | 2025-11-20 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 4227aeb1-dd2c-9ca1-e063-6294a90ad709 | 2025-11-20 | Warnings | M013 |
| good sense pain relief | ACETAMINOPHEN | NuCare Pharamceuticals, Inc. | 440c13d7-edf0-f611-e063-6394a90af995 | 2025-11-20 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 4227a2cc-69fa-869d-e063-6294a90a1d41 | 2025-11-20 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 422796ed-7558-f7e8-e063-6294a90ad1c7 | 2025-11-20 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 3e61abe4-b4be-01af-e063-6394a90a8b24 | 2025-11-20 | Warnings | M013 |
| Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | HYVEE INC | 3e60703b-a5cf-333a-e063-6394a90a2087 | 2025-11-20 | Warnings | M013 |
| ASPIRIN | ASPIRIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 54e4ae54-caf8-4105-8428-256f56a2f68f | 2025-11-19 | Warnings | M013 |
| MIDOL COMPLETE | ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE | R J General Corporation | 0c09a178-1a07-4079-b4a6-d1657cb8e714 | 2025-11-17 | Warnings | M013 |
| Alka-Seltzer Original | ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE | R J General Corporation | dbb0d067-71f0-45e4-bc98-548cf4a90b3a | 2025-11-17 | Warnings | M013 |
| MOTRIN IB | IBUPROFEN | R J General Corporation | afa87bb5-7fcb-4ccd-acac-f7931242181f | 2025-11-17 | Warnings | M013 |
| TYLENOL EXTRA STRENGTH | ACETAMINOPHEN | R J General Corporation | 99e45e83-37a3-44df-9a2a-98ba7457a5bb | 2025-11-17 | Warnings | M013 |
| TYLENOL PM EXTRA STRENGTH | ACETAMINOPHEN | R J General Corporation | a40ea0e3-d666-4605-b5e0-beeaf8f586f2 | 2025-11-17 | Warnings | M013 |
| Acetaminophen 250 mg and Ibuprofen 125 mg | ACETAMINOPHEN 250 MG AND IBUPROFEN 125 MG | R J General Corporation | 68d3be55-9340-4cc9-a05a-12b9338ddc56 | 2025-11-17 | Warnings | M013 |
| Ibuprofen 200 mg | IBUPROFEN | R J General Corporation | dd9aaf80-6c2b-41a3-87b9-61642aaed4f0 | 2025-11-17 | Warnings | M013 |
| Ibuprofen 200 mg | IBUPROFEN | R J General Corporation | 1c18a2da-1718-4c00-aea8-9fb4a3418312 | 2025-11-17 | Warnings | M013 |
| Ibuprofen 200 mg | IBUPROFEN | R J General Corporation | cd3060a5-3b90-42e4-89cd-3b620859045f | 2025-11-17 | Warnings | M013 |
| Ibuprofen 200 mg | IBUPROFEN | R J General Corporation | 1c7221ae-52d1-4d18-b586-c47ff656150d | 2025-11-17 | Warnings | M013 |
| Excedrin Extra Strength Headache | ACETAMINOPHEN, ASPIRIN (NSAID), CAFFEINE | R J General Corporation | 907c89e7-2482-465f-9f85-2381ecab1b86 | 2025-11-17 | Warnings | M013 |
| Bayer Genuine Aspirin | ASPIRIN | R J General Corporation | 23daa359-d40f-4f64-81be-6d154f41df9f | 2025-11-17 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198440 | acetaminophen 500 MG Oral Tablet | PSN | e677f43d-b4ce-e5b0-e053-2a95a90ad67e | 12 |
| 198440 | acetaminophen 500 MG Oral Tablet | SCD | e677f43d-b4ce-e5b0-e053-2a95a90ad67e | 12 |
| 198440 | APAP 500 MG Oral Tablet | SY | e677f43d-b4ce-e5b0-e053-2a95a90ad67e | 12 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 82706-007-01 | 82706000701 | 1 BOTTLE, PLASTIC in 1 CARTON (82706-007-01) / 24 TABLET in 1 BOTTLE, PLASTIC | 2022-08-17 | 0000-00-00 | No | No | Current | |
| 82706-007-02 | 82706000702 | 1 BOTTLE, PLASTIC in 1 CARTON (82706-007-02) / 100 TABLET in 1 BOTTLE, PLASTIC | 2022-08-17 | 0000-00-00 | No | No | Current | |
| 82706-007-03 | 82706000703 | 400 TABLET in 1 BOTTLE, PLASTIC (82706-007-03) | 400 tablet | 2022-08-17 | 0000-00-00 | No | No | Current |
| 82706-007-04 | 82706000704 | 3 POUCH in 1 CARTON (82706-007-04) / 2 TABLET in 1 POUCH | 3 pouch | 2023-09-20 | No | No | Current | |
| 82706-007-05 | 82706000705 | 50 POUCH in 1 CARTON (82706-007-05) / 2 TABLET in 1 POUCH | 50 pouch | 2024-07-05 | No | No | Current | |
| 82706-007-06 | 82706000706 | 25 BLISTER PACK in 1 CARTON (82706-007-06) / 25 TABLET in 1 BLISTER PACK | 25 blister pack | 2025-02-12 | No | No | Current |