good sense allergy relief
- Product NDC
- 0113-0479
- 11-digit product format
- 001130479
- Labeler code
- 0113
- Product ID
- 0113-0479_76ee13f5-338f-4c02-89f0-4a862333353e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1991-08-20
- 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
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 | 0113-0479 | 0113-0479-53 | D | Discontinued by firm | 2026-10-23 | |
| excluded package | package | 0113-0479 | 0113-0479-62 | D | Discontinued by firm | 2026-10-23 | |
| excluded package | package | 0113-0479 | 0113-0479-67 | D | Discontinued by firm | 2026-10-23 |
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 | 0113-0479-53 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | 0113-0479-67 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | 0113-0479-53 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | 0113-0479-67 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 0113-0479-53 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 0113-0479-67 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | 0113-0479-53 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | 0113-0479-67 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | 0113-0479-53 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | 0113-0479-67 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | 0113-0479-53 | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | 0113-0479-67 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 0113-0479-53 | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 0113-0479-67 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | 0113-0479-53 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | 0113-0479-67 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0113-0479-53 | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0113-0479-67 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | 0113-0479-53 | ad56d346431e… | cc804d4bbf1e… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | 0113-0479-67 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 0113-0479-53 | 367a005e9d99… | 383a685ebd0f… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 0113-0479-67 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 0113-0479-53 | 557ba5c1ecfa… | 9c80585c8c6e… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 0113-0479-67 | 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
- good sense allergy relief
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg/1 |
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 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0113-0479-53 | good sense allergy relief | 1 in 1 BLISTER PACK | TABLET | 1 | 9 | |
| 0113-0479-53 | good sense allergy relief | 12 in 1 CARTON | TABLET | 12 | 9 | |
| 0113-0479-62 | good sense allergy relief | 24 in 1 CARTON | TABLET | 24 | 9 | |
| 0113-0479-62 | good sense allergy relief | 1 in 1 BLISTER PACK | TABLET | 1 | 9 | |
| 0113-0479-67 | good sense allergy relief | 48 in 1 CARTON | TABLET | 48 | 9 | |
| 0113-0479-67 | good sense allergy relief | 1 in 1 BLISTER PACK | TABLET | 1 | 9 | |
| 0113-0479-78 | good sense allergy relief | 100 in 1 BOTTLE | TABLET | 100 | 9 | |
| 0113-0479-78 | good sense allergy relief | 1 in 1 CARTON | TABLET | 1 | 9 | |
| 0113-0479-79 | good sense allergy relief | 400 in 1 BOTTLE | TABLET | 400 | 9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0113-0479-53 | EA - Each | 0113-0479 | ee7a9bd6-c9e5-4049-a57f-f0df7b23a1c9 | 1 | 2018-02-20 |
| 0113-0479-62 | EA - Each | 0113-0479 | 8f6a54c4-4fa6-4bf7-a24a-10810f8a4ac4 | 1 | 2013-02-13 |
| 0113-0479-78 | EA - Each | 0113-0479 | d935c09b-7aa6-4a73-a496-1316061e7921 | 1 | 2013-02-13 |
| 0113-0479-79 | EA - Each | 0113-0479 | 4a7a8732-c938-489c-a655-e838ed920300 | 1 | 2020-09-14 |
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 |
|---|---|---|---|---|---|---|
| SF Honey Lemon Cough Drops | MENTHOL | The Kroger Co. | 43281bd1-f8a7-02a4-e054-00144ff8d46c | 2025-12-17 | Warnings | M012 |
| Kroger Cherry Cough Drops | MENTHOL | Kroger | a2e1d1f5-9b19-1704-e053-2a95a90abb51 | 2025-12-17 | Warnings | M012 |
| Tussin Multi Symptom Cold CF Adult | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE | Major Pharmaceuticals | a9958b7d-7060-422b-a098-c1925c246081 | 2025-12-17 | Warnings | M012 |
| Childrens Mucus Relief Cough Cherry Liquid | DEXTROMETHORPHAN HBR, GUAIFENSIN | Topco Associates | 3170748e-b09f-4c07-9927-df43771166c5 | 2025-12-16 | Warnings | M012 |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | ca6d43cf-0d1f-4d3c-be7e-e3ac6a24f4fe | 2025-12-16 | Warnings | M012 |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | e70d0784-53bc-4910-aade-3c9ad6e36441 | 2025-12-16 | Warnings | M012 |
| Pain and Sinus | ACETAMINOPHEN AND PHENYLEPHRINE | JHK Inc dba American Safety & First Aid | 88f86f5a-cc2b-4c75-b7a4-f2021922280b | 2025-12-16 | Warnings | M012 |
| Severe Congestion and Cough, Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, TRIPROLIDINE HCL | Walgreen Company | b75af815-9bd4-4a7a-bc68-f42f4af50699 | 2025-12-16 | Warnings | M012 |
| Cough Relief Nighttime | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | QUALITY CHOICE (Chain Drug Marketing Association) | fe5fd29e-7f81-4633-8c3b-010d68abe701 | 2025-12-16 | Warnings | M012 |
| Mucus Relief Severe Congestion and Cough Maximum Strength | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Harris Teeter, LLC | e0a62fa1-9f8a-4770-b28b-1f4f02a762e0 | 2025-12-16 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HCL | Walgreen Company | 8c4b59b8-dfab-4f4a-9966-f07b026a758a | 2025-12-16 | Warnings | M012 |
| Daytime Cold and Flu Non Drowsy | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | QUALITY CHOICE (Chain Drug Marketing Association) | df866cf6-0526-4e61-ac9b-245b57dd5df6 | 2025-12-16 | Warnings | M012 |
| Severe Cold and Flu Relief Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Walgreens | c89200b6-4adb-452e-b931-07f631dad641 | 2025-12-16 | Warnings | M012 |
| ONESSIP ADULT DAYTIME SEVERE COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI | MEDWISE LIFESCIENCES INC. | 45fa9159-d74c-063a-e063-6294a90a3ed0 | 2025-12-15 | Warnings | M012 |
| SudoGest Nasal Decongestant | PSEUDOEPHEDRINE HCL | Major Pharmaceuticals | 5229f4b2-a194-46f8-a0bc-4510fbe52075 | 2025-12-15 | Warnings | M012 |
| Topcare Nasal | OXYMETAZOLINE HYDROCHLORIDE | Topco Associates LLC | f2b2467f-2d9b-4742-b90a-95975c3b694f | 2025-12-13 | Warnings | M012 |
| Menthol Cough Drop | MENTHOL | HEB | 39178eb7-ada9-30bf-e054-00144ff88e88 | 2025-12-13 | Warnings | M012 |
| SF Menthol Cough Drop | MENTHOL | HEB | 3a443179-b7a6-3242-e054-00144ff8d46c | 2025-12-13 | Warnings | M012 |
| Cherry cough drop | MENTHOL | HEB | 39bd0ca1-348f-0ce1-e054-00144ff88e88 | 2025-12-13 | Warnings | M012 |
| Strawberry Cough Drops | MENTHOL | HEB | 766236e2-3302-2232-e053-2991aa0af503 | 2025-12-13 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049630 | diphenhydrAMINE HCl 25 MG Oral Tablet | PSN | 2cfa69b4-e33f-442a-a6df-b021b041da14 | 9 |
| 1049630 | diphenhydramine hydrochloride 25 MG Oral Tablet | SCD | 2cfa69b4-e33f-442a-a6df-b021b041da14 | 9 |
| 1049630 | diphenhydrAMINE HCl 25 MG Oral Tablet | PSN | 4d0f4f5b-3135-4457-bb8f-ad9d28ca5ea4 | 5 |
| 1049630 | diphenhydramine hydrochloride 25 MG Oral Tablet | SCD | 4d0f4f5b-3135-4457-bb8f-ad9d28ca5ea4 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0113-0479-53 | 00113047953 | 12 BLISTER PACK in 1 CARTON (0113-0479-53) > 1 TABLET in 1 BLISTER PACK | 12 blister pack | 2016-08-10 | 0000-00-00 | No | No | Current |
| 0113-0479-62 | 00113047962 | 1 BOTTLE in 1 CARTON (0113-0479-62) > 24 TABLET in 1 BOTTLE | 1 bottle | 1991-08-20 | 0000-00-00 | No | No | Current |
| 0113-0479-67 | 00113047967 | 48 BLISTER PACK in 1 CARTON (0113-0479-67) > 1 TABLET in 1 BLISTER PACK | 48 blister pack | 2021-06-04 | 0000-00-00 | No | No | Current |
| 0113-0479-78 | 00113047978 | 1 BOTTLE in 1 CARTON (0113-0479-78) / 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 1993-10-06 | 0000-00-00 | No | No | Current |
| 0113-0479-79 | 00113047979 | 400 TABLET, FILM COATED in 1 BOTTLE (0113-0479-79) | 2001-02-26 | 0000-00-00 | No | No | Current |