Overview
No overview information available.
Indication
No FDA- or EMA-approved therapeutic indications on its own.
Associated Conditions
- Conjunctivitis
- Stye
- Ulceration of the mouth
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Peaceful Mountain, Inc. | 43846-0039 | TOPICAL | 30 [hp_X] in 1 g | 5/21/2025 | |
King Bio Inc. | 57955-1814 | ORAL | 12 [hp_X] in 236 mL | 5/20/2025 |
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 |
---|---|---|---|---|---|
Kids Multi | 329564 | Medicine | A | 2/6/2020 | |
METAGENICS ENERGYX TROPICAL FLAVOUR | 343670 | Medicine | A | 9/17/2020 | |
Daily Multi Multivitamin | 337216 | Medicine | A | 5/29/2020 | |
Quality Health Australia Daily Multi | 404880 | Pharmacare Laboratories Pty Ltd | Medicine | A | 2/15/2023 |
ElementAll Diet | 447331 | Medicine | A | 5/1/2024 | |
Calcium For Healthy Bones | 447954 | Medicine | A | 5/7/2024 | |
Daily Multi Multivitamin | 443352 | Medicine | A | 3/7/2024 | |
COLLAGENICS | 122467 | Medicine | A | 10/6/2005 | |
NUTRA-LIFE JOINT FORMULA + MSM UNFLAVOURED POWDER | 284718 | Medicine | A | 1/17/2017 | |
METAGENICS HIGH STRENGTH BIOESSENTIALS | 445599 | Medicine | A | 4/10/2024 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
HOMEOPATHIC MEDICINE (S41) DPS 30C | total health centre | 02071266 | Drops - Oral | 30 C / ML | 12/31/1994 |
SORNIX | terra botanica products ltd. | 02233368 | Liquid - Oral | 30 X | 5/25/1998 |
CONSOLIN | dolisos laboratoires s.a. | 02242708 | Syrup - Oral | 5 CH / 25 ML | 3/9/2001 |
OPTREX EYE DROPS | schering-plough healthcare products canada, a division of schering canada inc. | 02236576 | Drops - Ophthalmic | 0.215 % | 8/20/1998 |
BORAX-INJEEL LIQ (8D,12D,30D,200D/1.1ML) | 02070529 | Liquid - Oral | 8 D / 1.1 ML | 12/31/1994 | |
BORAX GOUTTE 1CH - 30CH | boiron laboratoires | 00686670 | Drops - Oral | 1 CH / CH | 12/31/1987 |
BORAX GRANULE 1CH-30CH | homeocan inc. | 00890340 | Tablet - Oral | 1 CH | 12/31/1991 |
OPTREX EYE DROPS | knoll pharma inc. | 02185482 | Drops - Ophthalmic | 0.215 % | 12/31/1996 |
BORA-BOSAN B53-DPS | professional health products | 02157810 | Drops - Oral | 3 D / ML | 12/31/1996 |
P SHAMPOO | terra botanica products ltd. | 02233357 | Liquid - Topical | 12 X | 5/25/1998 |
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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