EBOLA REMEDY
- Product NDC
- 43742-0513
- 11-digit product format
- 437420513
- Labeler code
- 43742
- Product ID
- 43742-0513_910330a0-332f-471c-aebb-b04ee7acd0a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Crotalus Horridus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-09-26
- Marketing end
- 2022-10-06
- Substance
- CROTALUS HORRIDUS HORRIDUS VENOM
- Active strength
- 8 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0513-1 | 43742051301 | 30 mL in 1 BOTTLE, DROPPER (43742-0513-1) | 30 ml | 2014-09-26 | 2022-10-06 | No | No | Current |