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NDC 59469-0104-10 apo-TUSS 4; 4; 4; 4; 6; 4; 4; 2 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL Details
apo-TUSS 4; 4; 4; 4; 6; 4; 4; 2 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL
apo-TUSS is a ORAL SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by PEKANA Naturheilmittel GmbH. The primary component is ARUM MACULATUM ROOT; BRYONIA DIOICA ROOT; CUPRIC ACETATE; GELSEMIUM SEMPERVIRENS ROOT; HEDERA HELIX FLOWERING TWIG; HORSERADISH; LACTUCA VIROSA WHOLE; PROTORTONIA CACTI.
Product Information
| NDC | 59469-0104 |
|---|---|
| Product ID | 59469-104_d0974a83-5638-481c-8b47-77c313f15dd1 |
| 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 | apo-TUSS |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Arum Maculatum Root, Bryonia Dioica Root, Protortonia Cacti, Cupric Acetate, Gelsemium sempervirens Root, Hedera helix Flowering Twig, Lactuca virosa, and Horseradish |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SOLUTION/ DROPS |
| Route | ORAL |
| Active Ingredient Strength | 4; 4; 4; 4; 6; 4; 4; 2 |
| Active Ingredient Units | [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL |
| Substance Name | ARUM MACULATUM ROOT; BRYONIA DIOICA ROOT; CUPRIC ACETATE; GELSEMIUM SEMPERVIRENS ROOT; HEDERA HELIX FLOWERING TWIG; HORSERADISH; LACTUCA VIROSA WHOLE; PROTORTONIA CACTI |
| Labeler Name | PEKANA Naturheilmittel GmbH |
| Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59469-0104-10 (59469010410)
| NDC Package Code | 59469-104-10 |
|---|---|
| Billing NDC | 59469010410 |
| Package | 1 BOTTLE, GLASS in 1 BOX (59469-104-10) / 50 mL in 1 BOTTLE, GLASS |
| Marketing Start Date | 2008-12-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |