GANMAOLING
- Product NDC
- 72030-002
- Requested package NDC
- 72030-002-01
- 11-digit product format
- 720300002
- Labeler code
- 72030
- Product ID
- 72030-002_43e72532-332c-65b7-e063-6294a90aca7a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN AND CHLORPHENIRAMINE MALEATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ANHUI DONGSHENGYOUBANG PHARMACEUTICAL CO., LTD.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-11-26
- Marketing end
- 2029-08-30
- Substance
- ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE
- Active strength
- 60; .667 mg/1; mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- 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 | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
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
- GANMAOLING
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACETAMINOPHEN | 60 mg/1 |
| CHLORPHENIRAMINE MALEATE | .667 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 362O9ITL9D | Internal UNII lookup |
| V1Q0O9OJ9Z | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1599133 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c757a03e-59ea-469c-970d-4bc62e73f36f | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d17a97fa-387f-690e-d2be-0083ab044a03 | Product name | 3 | 20170725 |
| 0fdb98e2-b951-a1ce-5715-2b187ba500ef | Product name | 4 | 20170718 |
| c6fba691-a132-4ede-95c6-f8c6bd696636 | Product name | 1 | 20150902 |
| c0200ab5-4954-454e-9676-30b741b245bd | Product name | 1 | 20150730 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72030-002-01 | 2025-11-18 | C162847 | 48780-1 | 2cef2736-70f4-d83d-e063-dadaa90ab31f | DRUG FACTS |
| 72030-002-01 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-70f4-d83d-e063-dadaa90ab31f | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72030-002-01 | GANMAOLING | 1 in 1 BOX | TABLET | 1 | 2 | |
| 72030-002-01 | GANMAOLING | 120 in 1 BOTTLE | TABLET | 120 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72030-002 | GANMAOLING (ACETAMINOPHEN AND CHLORPHENIRAMINE MALEATE) TABLET [ANHUI DONGSHENGYOUBANG PHARMACEUTICAL CO., LTD.] | 1 | Current NDC, Legacy NDC, 2 package rows | 20181130_c757a03e-59ea-469c-970d-4bc62e73f36f.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 |
|---|---|---|---|---|---|---|
| MUCOSA | GUAIFENESIN | TIME CAP LABORATORIES,INC | d34ef2e8-adc2-48e5-a572-e354937daec6 | 2023-11-02 | Warnings | M012 |
| Daytime Severe and Nighttime Severe cold and flu | DAYTIME SEVERE - ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN AND NIGHTTIME SEVERE-ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | TARGET CORPORATION | 09286d15-b63f-a9de-e063-6294a90ab948 | 2023-11-02 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | AMERIFOODS TRADING COMPANY | f6cece6c-23e4-7811-e053-6394a90a106a | 2023-11-02 | Warnings | M012 |
| Sinus Pressure plus Pain PE | ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE | RETAIL BUSINESS SERVICES , LLC. | eb64750f-19ac-655f-e053-2995a90a33b5 | 2023-11-02 | Warnings | M012 |
| Multi-Symptom Mapap Cold Formula | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Proficient Rx LP | 9bf81b26-38b4-486c-ae89-222119ce1a4f | 2023-11-01 | Warnings | M012 |
| Guaifenesin Syrup and Dextromethorphan | GUAIFENESIN SYRUP AND DEXTROMETHORPHAN | Natco Pharma USA LLC | ad9026f4-f0b6-4d02-aa44-f0460eeefc0e | 2023-11-01 | Warnings | M012 |
| Diphenhydramine HCl Oral Solution | DIPHENHYDRAMINE HYDROCHLORIDE | Natco Pharma USA LLC | 54b64354-ac10-42ff-a53d-96cef933a91a | 2023-11-01 | Warnings | M012 |
| children allergy relief dye free cherry | DIPHENHYDRAMINE HCL | A-S Medication Solutions | 5c6c1809-4c6f-4e8f-a5ae-9796e821d400 | 2023-11-01 | Warnings | M012 |
| Daytime and Nighttime Cherry Cold and Flu | DAYTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR NIGHTTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR, DOXYLAMINE SUCCINATE | TARGET CORPORATION | 0903b222-1a44-64aa-e063-6294a90abba0 | 2023-10-31 | Warnings | M012 |
| Ephrine Nose Drops | PHENYLEPHRINE HYDROCHLORIDE | Walgreens | b620eb9f-2caf-0942-e053-2a95a90ae48e | 2023-10-31 | Warnings | M012 |
| pseudoephedrine hydrochloride | PSEUDOEPHEDRINE HCL | A-S Medication Solutions | 204849d1-ac4b-4dbe-8769-fcb30291f880 | 2023-10-31 | Warnings | M012 |
| Daytime Cold and Flu Relief | DAYTIME COLD AND FLU RELIEF | TopCo Associates, LLC | d592fbb8-d4bf-444e-982e-edf6fe97dce4 | 2023-10-31 | Warnings | M012 |
| Nite Time Cold and Flu Relief | NITE TIME COLD AND FLU RELIEF | TopCo Associates, LLC | 407dc4ae-882d-4a49-8884-ef048bb404cf | 2023-10-31 | Warnings | M012 |
| 12 Hour Original Nasal Decongestant | NASAL SPRAY | Sheffield Pharmaceuticals LLC | cea0ce76-ae75-4484-a7c2-ff1086e9d8b0 | 2023-10-30 | Warnings | M012 |
| Mucosa DM | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | Magno-Humphries, Inc. | 3a5533fb-1c83-4b95-9cd2-9be663d3ff5f | 2023-10-27 | Warnings | M012 |
| Mucosa Guifenesin | GUAIFENESIN | Magno-Humphries, Inc. | 9d22c208-d0ae-8b6a-e053-2995a90ab90a | 2023-10-27 | Warnings | M012 |
| DG Health Cough Drops Cherry Flavor | MENTHOL | Dollar General Corporation | c7a603d8-72fb-9626-e053-2995a90a09ea | 2023-10-26 | Warnings | M012 |
| Allergy Relief 4 Hour | CHLORPHENIRAMINE MALEATE | Geri-Care Pharmaceutical Corp | 92d90b41-0627-121e-e053-2995a90a2df1 | 2023-10-26 | Warnings | M012 |
| Freegells Cough Drops Menthol Cherry | MENTHOL | Riclan S.A. | 8e471265-3594-451a-8921-f0db474abe85 | 2023-10-26 | Warnings | M012 |
| Freegells Cough Drops Menthol Eucalyptus | MENTHOL | Riclan S.A. | 1141593a-f3ba-4adf-b332-f9fcb0b5a013 | 2023-10-26 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1599133 | acetaminophen 60 MG / chlorpheniramine maleate 0.667 MG Oral Tablet | PSN | c757a03e-59ea-469c-970d-4bc62e73f36f | 2 |
| 1599133 | acetaminophen 60 MG / chlorpheniramine maleate 0.667 MG Oral Tablet | SCD | c757a03e-59ea-469c-970d-4bc62e73f36f | 2 |
| 1599133 | APAP 60 MG / Chlorpheniramine Maleate 0.667 MG Oral Tablet | SY | c757a03e-59ea-469c-970d-4bc62e73f36f | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72030-002-01 | 72030000201 | 1 BOTTLE in 1 BOX (72030-002-01) / 120 TABLET in 1 BOTTLE | 1 bottle | 2018-11-26 | 2029-08-30 | No | No | Current |