Animal Antigens
- Product NDC
- 44911-0452
- Requested package NDC
- 44911-0452-1
- 11-digit product format
- 449110452
- Labeler code
- 44911
- Product ID
- 44911-0452_dffe4384-07aa-4ecc-a7d9-9feba4e20d35
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Canary Feathers, Cat Hair, Cattle Epithelia, Chicken Feathers, Dog Epithelia, Duck Feathers, Gerbil Epithelia, Goat Epithelia, Goose Feathers, Guinea Pig Epithelia, Hamster Epithelia, Hog Epithelia, Horse Epithelia, Mouse Epithelia, Parakeet Feathers, Rabbit Epithelia, Rat Epithelia, Arsenicum Album, Nux Vomica, Phosphorus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-07-18
- Marketing end
- 0000-00-00
- Substance
- SERINUS CANARIA FEATHER; FELIS CATUS HAIR; BOS TAURUS SKIN; GALLUS GALLUS FEATHER; CANIS LUPUS FAMILIARIS SKIN; ANAS PLATYRHYNCHOS FEATHER; MERIONES UNGUICULATUS SKIN; CAPRA HIRCUS SKIN; ANSER ANSER FEATHER; CAVIA PORCELLUS SKIN; MESOCRICETUS AURATUS SKIN; SUS SCROFA SKIN; EQUUS CABALLUS SKIN; MUS MUSCULUS SKIN; MELOPSITTACUS UNDULATUS FEATHER; ORYCTOLAGUS CUNICULUS SKIN; RATTUS NORVEGICUS SKIN; ARSENIC TRIOXIDE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS
- Active strength
- 9 [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
- 2020-12-31
- 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 | 44911-0452 | 44911-0452-1 | 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… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
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 |
|---|---|---|---|---|---|---|---|---|
| 44911-0452-1 | 44911045201 | 30 mL in 1 BOTTLE, DROPPER (44911-0452-1) | 30 ml | 2018-07-18 | 0000-00-00 | No | No | Current |