equate pain relief pm
- Product NDC
- 79903-421
- 11-digit product format
- 799030421
- Labeler code
- 79903
- Product ID
- 79903-421_7626ebea-c511-412f-99cc-86799de10054
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, diphenhydramine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- WALMART INC.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-29
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 1000; 50 mg/30mL; mg/30mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- equate pain relief pm
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 1000 mg/30mL |
| DIPHENHYDRAMINE HYDROCHLORIDE | 50 mg/30mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
| TC2D6JAD40 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1092373 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 85129749-c1a7-4c4a-933f-c3c4768e2cdd | 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 |
|---|---|---|---|---|---|---|
| 79903-421-12 | equate pain relief pm | 355 mL in 1 BOTTLE | SOLUTION | 355 | 2 |
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 |
|---|---|---|---|---|---|---|
| Gemma Cut the Cramp | ASPIRIN, CAFFEINE | Rally Labs LLC | 16c9a296-077a-8e12-e063-6294a90a1b8b | 2025-12-29 | Warnings | M013 |
| Blowfish | ASPIRIN, CAFFEINE | Rally Labs LLC | 0d3798bc-04ef-584e-821b-7aa76036b7d1 | 2025-12-29 | Warnings | M013 |
| Pain Relief PM | ACETAMINOPHEN, DIPHENHYDRAMINE | Pioneer Life Sciences, LLC | ad29a37f-39a2-5c84-e053-2995a90a2f39 | 2025-12-29 | Warnings | M013 |
| Tension Headache Relief | ACETAMINOPHEN, CAFFEINE | Pioneer Life Sciences, LLC | ac9efd62-8fee-b777-e053-2995a90a3783 | 2025-12-29 | Warnings | M013 |
| Childrens Pain Relief and Fever Reducer Oral Suspension Cherry | ACETAMINOPHEN | Puro Pharma Inc. | a2afaee7-19f3-4a42-a5b8-1d0ef3ecf009 | 2025-12-27 | Warnings | M013 |
| Cystex PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Clarion Brands, LLC | 9668a2ca-729e-4172-80b5-33e6c5175ba4 | 2025-12-27 | Warnings | M013 |
| Excedrin Extra Strength Headache | ACETAMINOPHEN, ASPIRIN (NSAID), CAFFEINE | Select Consumer Group | 3caa0a47-de83-90d2-e063-6394a90a3436 | 2025-12-27 | Warnings | M013 |
| Aspirin Pain reliver | ASPIRIN | Pioneer Life Sciences, LLC | c2759844-a49c-450f-e053-2a95a90a2972 | 2025-12-26 | Warnings | M013 |
| Menstrual Complete | ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE | Pioneer Life Sciences, LLC | aa2de3a5-a20d-33c6-e053-2a95a90ada3e | 2025-12-26 | Warnings | M013 |
| Childrens Pain and Fever | ACETAMINOPHEN | Discount Drug Mart | 2aa0f9f3-924c-4a4a-bb5f-2a326acc2408 | 2025-12-26 | Warnings | M013 |
| GenCare Headache Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Pioneer Life Sciences, LLC | 667f6f1b-5179-481c-a131-940c7937aada | 2025-12-26 | Warnings | M013 |
| Pharbetol | ACETAMINOPHEN | Pharbest Pharmaceuticals, Inc. | 04dbd98f-c74d-43b2-8bda-74f18be7cf6c | 2025-12-24 | Warnings | M013 |
| Adult Low Dose Aspirin Enteric Coated | ASPIRIN 81MG | Pharbest Pharmaceuticals, Inc. | 45e5bae9-22a7-4699-85ea-5b922af6b96d | 2025-12-24 | Warnings | M013 |
| Aspirin 325 mg | ASPIRIN | BETTER LIVING BRANDS, LLC | 424a242f-c8c6-9dd7-e063-6394a90ab4d5 | 2025-12-24 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | Pharbest Pharmaceuticals, Inc. | 2763a733-d617-4d95-8429-fbf81d9d77fb | 2025-12-24 | Warnings | M013 |
| Pharbetol Regular strength | ACETAMINOPHEN | Pharbest Pharmaceuticals, Inc. | e0a39957-d918-4125-88f9-0e550b976fa1 | 2025-12-24 | Warnings | M013 |
| PHARBETOL | ACETAMINOPHEN 500MG | Pharbest Pharmaceuticals, Inc. | 27337be9-e279-460e-903e-ae4463099599 | 2025-12-24 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | PUBLIX SUPERMARKETS, INC | 08f5af1d-365b-a97c-e063-6394a90a99ae | 2025-12-23 | Warnings | M013 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | Pioneer Life Sciences, LLC | 0d67bb52-7ae3-439e-9e47-4e21eb0ca352 | 2025-12-23 | Warnings | M013 |
| ACETAMINOPHEN 500 MG | ACETAMINOPHEN | Pioneer Life Sciences, LLC | 11e6ec2a-5171-4496-a15f-6ff744bd1f2f | 2025-12-23 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1092373 | acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG in 15 mL Oral Solution | PSN | 85129749-c1a7-4c4a-933f-c3c4768e2cdd | 2 |
| 1092373 | acetaminophen 33.3 MG/ML / diphenhydramine hydrochloride 1.67 MG/ML Oral Solution | SCD | 85129749-c1a7-4c4a-933f-c3c4768e2cdd | 2 |
| 1092373 | acetaminophen 1000 MG / diphenhydramine HCl 50 MG per 30 ML Oral Solution | SY | 85129749-c1a7-4c4a-933f-c3c4768e2cdd | 2 |
| 1092373 | acetaminophen 500 MG / diphenhydramine HCl 25 MG per 15 ML Oral Solution | SY | 85129749-c1a7-4c4a-933f-c3c4768e2cdd | 2 |
| 1092373 | APAP 33.3 MG/ML / Diphenhydramine Hydrochloride 1.67 MG/ML Oral Solution | SY | 85129749-c1a7-4c4a-933f-c3c4768e2cdd | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 79903-421-12 | 79903042112 | 355 mL in 1 BOTTLE (79903-421-12) | 355 ml | 2026-04-29 | No | No | Current |