Acetaminophen PM
- Product NDC
- 55301-235
- 11-digit product format
- 553010235
- Labeler code
- 55301
- Product ID
- 55301-235_f7fb7025-847b-4902-97cd-ce5317267514
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ARMY AND AIR FORCE EXCHANGE SERVICE
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1994-05-15
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500; 25 mg/1; mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 55301-235 | 55301-235-06 | D | Discontinued by firm | 2026-10-16 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 55301-235 | 55301-235-06 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… |
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 PM
- Brand name suffix
- Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 500 mg/1 |
| DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
| TC2D6JAD40 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1092189 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| f1157dbc-d86c-4554-954c-60a74674ff6b | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| 3e48c9c4-918d-5d23-2f0b-d2398b06be54 | Product name | 1 | 20140508 |
| 865c72dd-0d94-daac-f728-ddd4ded2a79e | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55301-235-06 | Acetaminophen PMExtra Strength | 200 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 200 | 13 | |
| 55301-235-15 | Acetaminophen PMExtra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 13 | |
| 55301-235-15 | Acetaminophen PMExtra Strength | 50 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 50 | 13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 55301-235 | ACETAMINOPHEN PM EXTRA STRENGTH (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) TABLET, FILM COATED [ARMY AND AIR FORCE EXCHANGE SERVICE] | 12 | Current NDC, Legacy NDC, 3 package rows | 20241127_f1157dbc-d86c-4554-954c-60a74674ff6b.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 |
|---|---|---|---|---|---|---|
| Childrens Mapap | ACETAMINOPHEN | Major Pharmaceuticals | efec6af2-8b26-47f6-88c8-b0a6d69a2d7d | 2026-06-03 | Warnings | M013 |
| Acetaminophen PM Extra Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | United Natural Foods, Inc. dba UNFI | ae3114c3-8cfe-4b81-8ac7-c281fe68b462 | 2026-06-03 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | COSTCO WHOLESALE CORPORATION | 3745aa18-a711-43ed-9bc4-1f087b3c53c0 | 2026-06-03 | Warnings | M013 |
| TYLENOL Extra Strength | ACETAMINOPHEN | Kenvue Brands LLC | 3f653262-b931-7d42-e063-6394a90adddd | 2026-06-03 | Warnings | M013 |
| Pain Reliever | ACETAMINOPHEN | Walgreen Company | 0b1bef50-7957-4ea1-9ae3-91f59ea2dbb4 | 2026-06-03 | Warnings | M013 |
| Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | WALMART INC. | 42310898-cf3a-4ffb-88bb-b8b84449156e | 2026-06-02 | Warnings | M013 |
| PAIN RELIEF | ACETAMINOPHEN | Meijer, Inc. | 1319bab8-8f17-44fb-9d91-099b0ba38a8d | 2026-06-01 | Warnings | M013 |
| Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Family Dollar (FAMILY WELLNESS) | 7a98d4d9-54e2-45c1-a76a-7f1907566e95 | 2026-06-01 | Warnings | M013 |
| Extra Strength Acetaminophen | ACETAMINOPHEN | TIME CAP LABORATORIES, INC. | 58840cf4-aceb-c7cf-e063-6294a90a5ff4 | 2026-06-01 | Warnings | M013 |
| Childrens Pain and Fever | ACETAMINOPHEN | CVS Pharmacy | 832acd72-1dda-4490-978f-5f31748942df | 2026-06-01 | Warnings | M013 |
| Acetaminophen PM | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | Major Pharmaceuticals | 786dbcd5-f5c2-4491-e053-2991aa0a3437 | 2026-05-29 | Warnings | M013 |
| Back and Body Extra Strength | ASPIRIN, CAFFEINE | Meijer Distribution Inc | e513f2d9-d591-4790-a117-6176ce2279dc | 2026-05-29 | Warnings | M013 |
| Chewable Acetaminophen Childrens | ACETAMINOPHEN | Cardinal Health 110, LLC. DBA Leader | 5460a4b7-5da3-4fc2-a565-0b0dd11bbf44 | 2026-05-29 | Warnings | M013 |
| Extra Strength Mini Softgels Pain Reliever | ACETAMINOPHEN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | f55d3663-7007-41cd-ae2d-5aca6311be81 | 2026-05-28 | Warnings | M013 |
| Genexa Kids Pain and Fever | ACETAMINOPHEN | Genexa Inc. | 5130c695-a80e-2dd3-e063-6294a90a404f | 2026-05-28 | Warnings | M013 |
| TYLENOL Regular Strength | ACETAMINOPHEN | Kenvue Brands LLC | 1622f694-4d63-4c56-8737-fae31f0ecfb7 | 2026-05-27 | Warnings | M013 |
| INFANTS Pain and Fever | ACETAMINOPHEN | Aurohealth LLC | 257436e1-e0f3-4a87-bffe-4f176b836caf | 2026-05-27 | Warnings | M013 |
| Infants Pain and Fever | ACETAMINOPHEN | Aurohealth LLC | 6509a545-0036-460a-8f0d-b31caae17855 | 2026-05-27 | Warnings | M013 |
| Alka-Seltzer Original | ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE | Select Consumer Group | 3ca80d74-1e8b-49d9-e063-6394a90a4312 | 2026-05-24 | Warnings | M013 |
| Pain and Fever Chewables Childrens | ACETAMINOPHEN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | bad8ac0a-518d-4639-9b92-a39e0d437238 | 2026-05-22 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1092189 | acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet | PSN | f1157dbc-d86c-4554-954c-60a74674ff6b | 13 |
| 1092189 | acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet | SCD | f1157dbc-d86c-4554-954c-60a74674ff6b | 13 |
| 1092189 | APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet | SY | f1157dbc-d86c-4554-954c-60a74674ff6b | 13 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 55301-235-06 | 55301023506 | 200 TABLET, FILM COATED in 1 BOTTLE (55301-235-06) | 1994-05-15 | 0000-00-00 | No | No | Current |
| 55301-235-15 | 55301023515 | 1 BOTTLE, PLASTIC in 1 CARTON (55301-235-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1994-05-15 | 0000-00-00 | No | No | Current |