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NDC 69676-0049-01 Genexa Kids Cold Crush 12; 9; 6; 6; 12; 12; 6; 6; 9; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details
Genexa Kids Cold Crush 12; 9; 6; 6; 12; 12; 6; 6; 9; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Genexa Kids Cold Crush is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Genexa Inc.. The primary component is ACONITUM NAPELLUS; BRYONIA ALBA ROOT; ECHINACEA ANGUSTIFOLIA; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; MATRICARIA CHAMOMILLA WHOLE; ONION; PULSATILLA PRATENSIS; SAMBUCUS NIGRA FLOWER.
Product Information
| NDC | 69676-0049 |
|---|---|
| Product ID | 69676-0049_f5d860bd-d54d-42dd-e053-2995a90a2e54 |
| 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 | Genexa Kids Cold Crush |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Aconitum napellus, Allium cepa, Bryonia alba, Chamomilla, Echinacea angustifolia, Euphrasia officinalis, Gelsemium sempervirens, Ipecacuanha, Pulsatilla, Sambucus nigra |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, CHEWABLE |
| Route | ORAL |
| Active Ingredient Strength | 12; 9; 6; 6; 12; 12; 6; 6; 9; 6 |
| Active Ingredient Units | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Substance Name | ACONITUM NAPELLUS; BRYONIA ALBA ROOT; ECHINACEA ANGUSTIFOLIA; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; MATRICARIA CHAMOMILLA WHOLE; ONION; PULSATILLA PRATENSIS; SAMBUCUS NIGRA FLOWER |
| Labeler Name | Genexa Inc. |
| Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Vegetable Proteins [CS] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69676-0049-01 (69676004901)
| NDC Package Code | 69676-0049-1 |
|---|---|
| Billing NDC | 69676004901 |
| Package | 1 BOTTLE, PLASTIC in 1 CARTON (69676-0049-1) / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2020-07-31 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |