Search by Drug Name or NDC
NDC 69676-0006-01 Cold Crush Adult 6; 12; 6; 12; 6; 6; 12; 12; 12 [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
Cold Crush Adult 6; 12; 6; 12; 6; 6; 12; 12; 12 [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
Cold Crush Adult 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; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; ONION; PULSATILLA PRATENSIS; SCHOENOCAULON OFFICINALE SEED; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS SHOOT.
Product Information
| NDC | 69676-0006 |
|---|---|
| Product ID | 69676-0006_f5d9a016-4931-3eda-e053-2995a90a0300 |
| 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 | Cold Crush Adult |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Aconitum napellus, Allium cepa, Bryonia alba, Euphrasia officinalis, Gelsemium sempervirens, Nux vomica, Pulsatilla, Rhus toxicodendron, Sabadilla |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, CHEWABLE |
| Route | ORAL |
| Active Ingredient Strength | 6; 12; 6; 12; 6; 6; 12; 12; 12 |
| 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 |
| Substance Name | ACONITUM NAPELLUS; BRYONIA ALBA ROOT; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; ONION; PULSATILLA PRATENSIS; SCHOENOCAULON OFFICINALE SEED; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS SHOOT |
| Labeler Name | Genexa Inc. |
| Pharmaceutical Class | Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [E |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69676-0006-01 (69676000601)
| NDC Package Code | 69676-0006-1 |
|---|---|
| Billing NDC | 69676000601 |
| Package | 1 BOTTLE in 1 CARTON (69676-0006-1) / 60 TABLET, CHEWABLE in 1 BOTTLE |
| Marketing Start Date | 2018-07-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |