Overview
Honey is an animal extract used in some OTC (over-the-counter) products. It is not an approved drug.
Indication
补中，润燥，止痛，解毒。用于脘腹虚痛，肺燥干咳，肠燥便秘，解乌头类药毒；外治疮疡不敛，水火烫伤。
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2024/06/13 | Phase 1 | Recruiting | Watim Medical & Dental College | ||
2024/01/11 | Phase 4 | Completed | |||
2023/07/14 | Phase 4 | Completed | Hasanuddin University | ||
2021/08/27 | Phase 3 | Completed | Postgraduate Medical Institute, Lahore | ||
2021/04/19 | Early Phase 1 | Completed | |||
2021/04/05 | Not Applicable | Completed | |||
2021/02/23 | Phase 2 | UNKNOWN | |||
2020/06/11 | Phase 2 | Completed | |||
2020/04/15 | Phase 3 | Completed | |||
2020/03/03 | Phase 2 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Guangdong Bisutang Biotechnology Co., LTD | 84753-037 | TOPICAL | 0.001 mg in 100 g | 9/22/2025 | |
| Shantou Ximonth Biotechnology Co., Ltd. | 84989-011 | TOPICAL | 0.01 mg in 50 mg | 9/9/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| Kiwiherb ImmuneBerry | 332040 | Phytomed Australia Pty Ltd | Medicine | A | 3/23/2020 |
| Kiwiherb Echinature | 335157 | Phytomed Australia Pty Ltd | Medicine | A | 4/25/2020 |
| Manuka Honey Chesty Cough | 445564 | Medicine | A | 4/9/2024 | |
| Bioglan Medlab Manuka-C | 391036 | Medicine | A | 6/21/2022 | |
| Manuka Honey Dry Cough | 321825 | Medicine | A | 8/15/2019 | |
| Sambucol Black Elderberry Sore Throat + Cold & Flu | 441412 | Pharmacare Laboratories Pty Ltd | Medicine | A | 2/19/2024 |
| Herbal Throat Spray | 462254 | Phytomed Australia Pty Ltd | Medicine | A | 9/16/2024 |
| Sambucol Black Elderberry Immune Defence Kids | 368512 | Pharmacare Laboratories Pty Ltd | Medicine | A | 6/8/2021 |
| THERAPEUTIC SKIN CREAM with Active Manuka Honey | 152408 | Medicine | A | 5/16/2008 | |
| Look Mei Pills | 260520 | Medicine | A | 9/30/2015 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| MIELOCOL SYRUP | herbes universelles inc. | 00417149 | Syrup - Oral | .16 ML / 5 ML | 12/31/1966 |
| HERBAL COUGH EXPECTORANT | jamieson laboratories ltd | 02125811 | Syrup - Oral | 50.4 MG / 5 ML | 12/31/1994 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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