NDC 59469-066
KELAN
Silicon Dioxide, Arnica Montana Root, Graphite, Hypericum Perforatum, Ledum Palustre Twig, Magnesium Fluoride, Magnesium Sulfate Heptahydrate, And Ruta Graveolens Flowering Top
KELAN is a Cutaneous Ointment in the Human Otc Drug category. It is labeled and distributed by Pekana Naturheilmittel Gmbh. The primary component is Arnica Montana Root; Graphite; Hypericum Perforatum Whole; Magnesium Fluoride; Magnesium Sulfate Heptahydrate; Rhododendron Tomentosum Leafy Twig; Ruta Graveolens Flowering Top; Silicon Dioxide.
| Product ID | 59469-066_63d764d3-3f6c-4445-ac66-40ef9869b161 |
| NDC | 59469-066 |
| Product Type | Human Otc Drug |
| Proprietary Name | KELAN |
| Generic Name | Silicon Dioxide, Arnica Montana Root, Graphite, Hypericum Perforatum, Ledum Palustre Twig, Magnesium Fluoride, Magnesium Sulfate Heptahydrate, And Ruta Graveolens Flowering Top |
| Dosage Form | Ointment |
| Route of Administration | CUTANEOUS |
| Marketing Start Date | 2008-04-12 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | PEKANA Naturheilmittel GmbH |
| Substance Name | ARNICA MONTANA ROOT; GRAPHITE; HYPERICUM PERFORATUM WHOLE; MAGNESIUM FLUORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE |
| Active Ingredient Strength | 12 [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g |
| Pharm Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
Packaging
NDC 59469-066-30
1 TUBE in 1 BOX (59469-066-30) > 30 g in 1 TUBE
| Marketing Start Date | 2008-04-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 59469-066-35 [59469006635]
KELAN OINTMENT
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-04-12 |
NDC 59469-066-30 [59469006630]
KELAN OINTMENT
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2008-04-12 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| SILICON DIOXIDE | 6 [hp_X]/35g |
OpenFDA Data
| SPL SET ID: | 55786d99-ee1f-490f-9023-3e6c39da86b0 |
| Manufacturer | |
| UNII |
Trademark Results [KELAN]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KELAN 88538775 not registered Live/Pending |
Zeng Qiaoling 2019-07-26 |
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