Allergy Relief
- Product NDC
- 50844-329
- 11-digit product format
- 508440329
- Labeler code
- 50844
- Product ID
- 50844-329_c32f9c98-7532-4e52-b09d-45534043e8ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L.N.K. International, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1990-03-02
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- 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
- Allergy Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| TC2D6JAD40 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1049630 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| db264d2f-bf81-4da2-8595-2bfa1e4ba2f1 | 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 |
|---|---|---|---|---|---|---|
| 50844-329-02 | Allergy Relief | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 | |
| 50844-329-02 | Allergy Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 19 | |
| 50844-329-07 | Allergy Relief | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 | |
| 50844-329-07 | Allergy Relief | 3 in 1 CARTON | TABLET, FILM COATED | 3 | 19 | |
| 50844-329-08 | Allergy Relief | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 | |
| 50844-329-08 | Allergy Relief | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 19 | |
| 50844-329-12 | Allergy Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 19 | |
| 50844-329-22 | Allergy Relief | 4 in 1 CARTON | TABLET, FILM COATED | 4 | 19 | |
| 50844-329-22 | Allergy Relief | 12 in 1 BLISTER PACK | TABLET, FILM COATED | 12 | 19 | |
| 50844-329-51 | Allergy Relief | 365 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 365 | 19 | |
| 50844-329-78 | Allergy Relief | 600 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 600 | 19 | |
| 50844-329-82 | Allergy Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 19 | |
| 50844-329-82 | Allergy Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 19 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50844-329-07 | EA - Each | 50844-329 | 8e1ca771-4325-4b82-80ac-dfa62a1ac889 | 1 | 2025-10-14 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Basic Care Honey Lemon Cough Drops | MENTHOL | Amazon.com | c0937b13-f679-a764-e053-2a95a90abf89 | 2025-12-05 | Warnings | M012 |
| Basic Care SF Menthol Cough Drops | MENTHOL | Amazon.com | c0946295-7cf0-1bd8-e053-2a95a90af5af | 2025-12-05 | Warnings | M012 |
| Basic Care SF Honey Lemon Cough Drops | MENTHOL | Amazon.com | cf82fb0b-1b4d-def1-e053-2995a90a6fd9 | 2025-12-05 | Warnings | M012 |
| G-DOLOGEN | ACETAMINOPHEN, DEXBROMPHENIRAMINE MALEATE | Kramer Novis | 7a4e1d64-2510-405f-a1dc-e02a803b6fbd | 2025-12-05 | Warnings | M012 |
| Quality Choice Severe Cold and Cough Nighttime | ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE | Chain Drug Manufacturing Assn | ce658dd5-b683-436e-b16b-0c06f6f87fd9 | 2025-12-04 | Warnings | M012 |
| Quality Choice Maximum Strength | OXYMETAZOLINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION | a87ba15f-b5a9-4983-a721-ca7f705aea86 | 2025-12-04 | Warnings | M012 |
| Quality Choice | PHENYLEPHRINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION | a12e2e66-d2f3-47a6-a915-a309ae828d27 | 2025-12-04 | Warnings | M012 |
| Childrens Mucus Relief Chest Congestion | GUAIFENESIN | Chain Drug Manufacturing Assn | 034d39c0-9aad-4dff-a158-a041b9f0504f | 2025-12-04 | Warnings | M012 |
| Quality Choice | OXYMETAZOLINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION | d01b8fb6-1ddf-4901-bda6-ae608e94a6a4 | 2025-12-04 | Warnings | M012 |
| Childrens Mucus and Cough Relief | GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE | Chain Drug Manufacturing Assn | 06822a28-3f82-471d-8db5-c5981b263a03 | 2025-12-04 | Warnings | M012 |
| QUALITY CHOICE | PHENYLEPHRINE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION | 14596551-dd82-46b3-8eb8-e69efaea105b | 2025-12-04 | Warnings | M012 |
| Daytime Cold and Flu Lil Drug Store Products | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Lil' Drug Store Products, Inc | fd5c20ed-5520-4db0-bfd4-995f043af2a4 | 2025-12-04 | Warnings | M012 |
| Afrin Original | OXYMETAZOLINE HYDROCHLORIDE | Bayer HealthCare LLC. | 89c165ba-3ad5-49b5-a5bb-423dc8e15bad | 2025-12-04 | Warnings | M012 |
| Alka-Seltzer Plus Severe Cold Powerfast Fizz Night | ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE BITARTRATE | Bayer HealthCare LLC. | a2b30c27-b836-f09f-e053-2995a90ac383 | 2025-12-04 | Warnings | M012 |
| Alka-Seltzer Plus Severe Cold PowerFast Fizz | ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE, DOXYLAMINE SUCCINATE | Bayer HealthCare LLC. | a37c9d9d-52db-23ff-e053-2995a90a8f76 | 2025-12-04 | Warnings | M012 |
| Alka-Seltzer Plus Severe Cold and Cough PowerFast Fizz | ASPIRIN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE | Bayer Healthcare LLC. | dd7d8a8c-0f91-5ef1-e053-2a95a90a3c6a | 2025-12-04 | Warnings | M012 |
| Alka-Seltzer Plus Cough, Mucus and Congestion Day and Night Powermax | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | a68df74d-dd26-3ae9-e053-2995a90a08d6 | 2025-12-04 | Warnings | M012 |
| Circle K Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Lil' Drug Store Products, Inc. | 55662ada-677e-4048-9529-5bca44076316 | 2025-12-04 | Warnings | M012 |
| Alka-Seltzer Plus Maximum Strength Day and Night Cold and Flu | DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE | Bayer HealthCare LLC. | b13d5132-cb91-3cf6-e053-2a95a90aa47c | 2025-12-04 | Warnings | M012 |
| Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | bd97e91f-1ae1-379c-e053-2995a90acfdd | 2025-12-04 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049630 | diphenhydrAMINE HCl 25 MG Oral Tablet | PSN | db264d2f-bf81-4da2-8595-2bfa1e4ba2f1 | 19 |
| 1049630 | diphenhydramine hydrochloride 25 MG Oral Tablet | SCD | db264d2f-bf81-4da2-8595-2bfa1e4ba2f1 | 19 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50844-329-02 | 50844032902 | 1 BLISTER PACK in 1 CARTON (50844-329-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 1990-03-02 | 0000-00-00 | No | No | Current |
| 50844-329-07 | 50844032907 | 3 BLISTER PACK in 1 CARTON (50844-329-07) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 1990-03-02 | 0000-00-00 | No | No | Current |
| 50844-329-08 | 50844032908 | 2 BLISTER PACK in 1 CARTON (50844-329-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 1990-03-02 | 0000-00-00 | No | No | Current |
| 50844-329-12 | 50844032912 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-12) | 1990-03-02 | No | No | Current | ||
| 50844-329-22 | 50844032922 | 4 BLISTER PACK in 1 CARTON (50844-329-22) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 4 blister pack | 1990-03-02 | 0000-00-00 | No | No | Current |
| 50844-329-51 | 50844032951 | 365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-51) | 1990-03-02 | No | No | Current | ||
| 50844-329-78 | 50844032978 | 600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-78) | 1990-03-02 | No | No | Current | ||
| 50844-329-82 | 50844032982 | 1 BOTTLE, PLASTIC in 1 CARTON (50844-329-82) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1990-03-02 | No | No | Current |