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NDC 59469-0066-35 KELAN 12; 6; 6; 12; 12; 12; 12; 6 [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g Details
KELAN 12; 6; 6; 12; 12; 12; 12; 6 [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g
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 Information
| NDC | 59469-0066 |
|---|---|
| Product ID | 59469-066_63d764d3-3f6c-4445-ac66-40ef9869b161 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | KELAN |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Silicon Dioxide, Arnica montana Root, Graphite, Hypericum Perforatum, Ledum Palustre Twig, Magnesium fluoride, Magnesium Sulfate Heptahydrate, and Ruta graveolens Flowering Top |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | OINTMENT |
| Route | CUTANEOUS |
| Active Ingredient Strength | 12; 6; 6; 12; 12; 12; 12; 6 |
| Active Ingredient Units | [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g; [hp_X]/35g |
| Substance Name | ARNICA MONTANA ROOT; GRAPHITE; HYPERICUM PERFORATUM WHOLE; MAGNESIUM FLUORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE |
| Labeler Name | PEKANA Naturheilmittel GmbH |
| Pharmaceutical Class | 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 |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59469-0066-35 (59469006635)
| NDC Package Code | 59469-066-35 |
|---|---|
| Billing NDC | 59469006635 |
| Package | 1 TUBE in 1 BOX (59469-066-35) / 35 g in 1 TUBE |
| Marketing Start Date | 2008-04-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |