Recalibr8
- Product NDC
- 73448-0001
- Requested package NDC
- 73448-0001-1
- 11-digit product format
- 734480001
- Labeler code
- 73448
- Product ID
- 73448-0001_6ef3de46-cb81-4bb0-91f4-f96586f2b309
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hypophysis Suis, Hypothalamus Suis, Aconitum Napellus, Aloe, Alumina, Antimonium Crudum, Apis Mellifica, Argentum Nitricum, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia (Alba), Calcarea Fluorica, Calendula Officinalis, Causticum, Chamomilla, Chelidonium Majus, Cistus Canadensis, Clematis Erecta, Ferrum Phosphoricum, Gambogia, Graphites, Histaminum Hydrochloricum, Hydrastis canadensis, Hydrofluoricum Acidum, Hypericum Perforatum, Ignatia amara, Impatiens Glandulifera, Flos,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Body Wisdom Center for Healing
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-03-11
- Marketing end
- 0000-00-00
- Substance
- SUS SCROFA PITUITARY GLAND; SUS SCROFA HYPOTHALAMUS; ACONITUM NAPELLUS WHOLE; ALOE; ALUMINUM OXIDE; ANTIMONY TRISULFIDE; APIS MELLIFERA; SILVER NITRATE; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; CALCIUM FLUORIDE; CALENDULA OFFICINALIS FLOWERING TOP; CAUSTICUM; MATRICARIA CHAMOMILLA WHOLE; CHELIDONIUM MAJUS WHOLE; HELIANTHEMUM CANADENSE; CLEMATIS RECTA FLOWERING TOP; FERROSOFERRIC PHOSPHATE; GAMBOGE; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; HYDROFLUORIC ACID; HYPERICUM PERFORATUM WHOLE; STRYCHNOS IGNATII SEED; IMPATIENS GLANDULIFERA FLOWER; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; NITRIC ACID; ORNITHOGALUM UMBELLATUM WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; LEAD; PRUNUS CERASIFERA FLOWER; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR; COMFREY ROOT; ALLYLTHIOUREA; VERATRUM ALBUM ROOT
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 73448-0001 | 73448-0001-1 | D | Discontinued by firm | 2026-10-05 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 73448-0001-1 | 73448000101 | 30 mL in 1 BOTTLE, SPRAY (73448-0001-1) | 30 ml | 2020-03-11 | 0000-00-00 | No | No | Current |