Allergy Relief
- Product NDC
- 49035-929
- 11-digit product format
- 490350929
- Labeler code
- 49035
- Product ID
- 49035-929_7eaae612-91c1-4789-a5ec-183149c2fb6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wal-Mart Stores 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
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 | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | 49035-929-12 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | 49035-929-12 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 49035-929-12 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | 49035-929-12 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | 49035-929-12 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | 49035-929-12 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 49035-929-12 | 302b2466d912… | e7b80fea0513… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 49035-929-51 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | 49035-929-51 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 49035-929-51 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 49035-929-51 | 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
- 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 |
|---|---|
| 150b68ba-3ed4-4533-9118-74e76eaf6e48 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| 594e2c86-3079-4e6e-96c9-48f7a8afc78d | Product name | 1 | 20230718 |
| 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 |
|---|---|---|---|---|---|---|
| 49035-929-12 | Allergy Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 17 | |
| 49035-929-12 | Allergy Relief | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 17 | |
| 49035-929-51 | Allergy Relief | 365 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 365 | 17 | |
| 49035-929-98 | Allergy Relief | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 17 | |
| 49035-929-98 | Allergy Relief | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 17 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49035-929-12 | EA - Each | 49035-929 | f1d450c6-3d47-43e9-ad96-17f5743b9eba | 1 | 2018-07-03 |
| 49035-929-51 | EA - Each | 49035-929 | 03c08122-71ad-4e38-b593-57d81d43cbef | 1 | 2019-11-12 |
| 49035-929-98 | EA - Each | 49035-929 | 1e9ff7d2-27b0-4b71-8b05-ee1c0fbdfb2d | 1 | 2023-04-07 |
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 |
|---|---|---|---|---|---|---|
| Medi-First Sinus Decongestant | PHENYLEPHRINE HYDROCHLORIDE | Unifirst First Aid Corporation | 9654f5cd-74d7-44a2-9674-666d1e94ffa7 | 2025-09-08 | Warnings | M012 |
| Otis Clapp Mygrex | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE | Unifirst First Aid Corporation | f196f2c5-a100-42b1-bd01-0327b223838e | 2025-09-08 | Warnings | M012 |
| Medique Diphen | DIPHENHYDRAMINE HYDROCHLORIDE | Unifirst First Aid Corporation | b61ee2e0-2543-447d-9fc4-23363d46ce04 | 2025-09-08 | Warnings | M012 |
| Green Guard Allergy 2 Relief | PHENYLEPHRINE HYDROCHLORIDE | Unifirst First Aid Corporation | 16fddca9-a66b-41e6-9423-eaf091d3971e | 2025-09-08 | Warnings | M012 |
| Medique Medi-Phenyl | PHENYLEPHRINE HYDROCHLORIDE | Unifirst First Aid Corporation | d7d62ac1-1333-4366-884b-26537766ce38 | 2025-09-08 | Warnings | M012 |
| Unishield Sinus Decongestant | PHENYLEPHRINE HCL | Unishield | b8f68d9d-2d38-414a-e053-2a95a90a15ec | 2025-09-08 | Warnings | M012 |
| McKesson Sinus Pain and Pressure Relief | ACETAMINOPHEN, PHENYLEPHRINE HCL | McKesson Medical-Surgical | e0cbb213-4f4f-4045-e053-2a95a90a2a18 | 2025-09-08 | Warnings | M012 |
| Medique Medicidin D | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE | Unifirst First Aid Corporation | 1f172d58-4050-424b-9743-130d8e618fe8 | 2025-09-08 | Warnings | M012 |
| Medique Cold Cough Product | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL , | Unifirst First Aid Corporation | e8059137-efba-398c-e053-2a95a90a21f2 | 2025-09-08 | Warnings | M012 |
| Medique Medi-Mucus | DEXTROMETHORPHAN HBR, GUAIFENESIN | Unifirst First Aid Corporation | f3bb862a-9cb8-f644-e053-2a95a90a5f4f | 2025-09-08 | Warnings | M012 |
| Physicians Care Cough and Sore Throat | MENTHOL | Acme United Corporation | 4e02223d-f34b-333e-e054-00144ff8d46c | 2025-09-08 | Warnings | M012 |
| Physicians Care Non-Drowsy Cold and Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Acme United | 186ec543-1f23-75d6-e063-6294a90a46b9 | 2025-09-08 | Warnings | M012 |
| PhysiciansCare Sinus Non-Drowsy | PHENYLEPHRINE HCL | Acme United Corporation | a6daf3ef-f386-4de4-b38e-d0b90c9ae62b | 2025-09-08 | Warnings | M012 |
| PhysiciansCare Allergy Multi-Symptom Relief | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE | Acme United Corporation | fd101c27-6ba9-4cd3-baec-a354504c37a0 | 2025-09-08 | Warnings | M012 |
| Green Guard Honey Lemon Cough Drop | MENTHOL 8.6 MG | Unifirst First Aid Corporation | 8a94f090-61d6-4909-e053-2995a90aee38 | 2025-09-08 | Warnings | M012 |
| Green Guard Cough Drop Relief | MENTHOL | Unifirst First Aid Corporation | 0fc4cb11-8ff9-4eff-9588-c73eef4e0137 | 2025-09-08 | Warnings | M012 |
| Multi-Symptom Cold Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL , GUAIFENESIN, , | Unifirst First Aid Corporation | e6ea6faf-baff-a130-e053-2a95a90a085a | 2025-09-08 | Warnings | M012 |
| MEDIQUE Medikoff Drops | MENTHOL | Unifirst First Aid Corporation | 0d6b4443-16a1-4851-bb03-d7407167551d | 2025-09-08 | Warnings | M012 |
| Medique Sugar Free Medikoff Drops | MENTHOL | Unifirst First Aid Corporation | 92d13e19-4e7b-4565-970e-504abf02579a | 2025-09-08 | Warnings | M012 |
| Medique at Home Diphen | DIPHENHYDRAMINE HCL | Unifirst First Aid Corporation | b56d1966-efd7-56eb-e053-2995a90a89b5 | 2025-09-08 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049630 | diphenhydrAMINE HCl 25 MG Oral Tablet | PSN | 150b68ba-3ed4-4533-9118-74e76eaf6e48 | 17 |
| 1049630 | diphenhydramine hydrochloride 25 MG Oral Tablet | SCD | 150b68ba-3ed4-4533-9118-74e76eaf6e48 | 17 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 49035-929-12 | 49035092912 | 1 BOTTLE, PLASTIC in 1 CARTON (49035-929-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1990-03-02 | 0000-00-00 | No | No | Current |
| 49035-929-51 | 49035092951 | 365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49035-929-51) | 1990-03-02 | 2023-05-18 | No | No | Current |
| 49035-929-98 | 49035092998 | 2 BOTTLE, PLASTIC in 1 CARTON (49035-929-98) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 1990-03-02 | 0000-00-00 | No | No | Current |