Spascupreel
- Product NDC
- 62795-9493
- 11-digit product format
- 627959493
- Labeler code
- 62795
- Product ID
- 62795-9493_3b7c25e7-6e4a-4670-9706-4abf3f61d4ed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACONITUM NAPELLUS WHOLE, AMANITA MUSCARIA FRUITING BODY, AMMONIUM BROMIDE, ATROPINE SULFATE, ATROPINE SULFATE, MATRICARIA CHAMOMILLA WHOLE, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC SULFATE,GELSEMIUM SEMPERVIRENS ROOT,MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE,PASSIFLORA INCARNATA FLOWERING TOP,VERATRUM ALBUM ROOT
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MediNatura Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2022-02-17
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS WHOLE; AMANITA MUSCARIA FRUITING BODY; AMMONIUM BROMIDE; ATROPINE SULFATE; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA CHAMOMILLA WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; VERATRUM ALBUM ROOT
- Active strength
- 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; [hp_X]/1
- Pharmacologic classes
- Anticholinergic [EPC], Calculi Dissolution Agent [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 62795-9493 | | I | Inactivated by FDA | | 2026-07-31 |
| excluded package | package | 62795-9493 | 62795-9493-2 | I | Inactivated by FDA | | 2026-07-31 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62795-9493-2 | Spascupreel | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 62795-9493-2 | Spascupreel | 1 in 1 CARTON | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62795-9493 | SPASCUPREEL (ACONITUM NAPELLUS WHOLE, AMANITA MUSCARIA FRUITING BODY, AMMONIUM BROMIDE, ATROPINE SULFATE, ATROPINE SULFATE, MATRICARIA CHAMOMILLA WHOLE, CITRULLUS COLOCYNTHIS FRUIT PULP, CUPRIC SULFATE,GELSEMIUM SEMPERVIRENS ROOT,MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE,PASSIFLORA INCARNATA FLOWERING TOP,VERATRUM ALBUM ROOT) TABLET [MEDINATURA INC] | 2 | Legacy NDC, 2 package rows | 20230515_854497b7-08a6-45ce-9761-cddb264b07dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62795-9493-2 | 62795949302 | 1 BOTTLE in 1 CARTON (62795-9493-2) > 100 TABLET in 1 BOTTLE | 1 bottle | 2022-02-17 | 0000-00-00 | No | No | Current |