Lymph Drainage
- Product NDC
- 43742-0236
- Requested package NDC
- 43742-0236-1
- 11-digit product format
- 437420236
- Labeler code
- 43742
- Product ID
- 43742-0236_ac2cfbbe-70d6-42b1-b8cf-2d4840676017
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Citrus Limonum, Echinacea, Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Lobelia Inflata, Phytolacca Decandra, Pinus Sylvestris, Zincum Gluconicum, Thuja Occidentalis, Capsicum Annuum, Cuprum Gluconicum, Manganum Gluconicum, Aranea Diadema, Arsenicum Iodatum, Centaury, Hornbeam, Larch, Lymph (Suis), Spleen (Suis), Thymus (Suis), Lachesis Mutus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-05-15
- Marketing end
- 2021-05-10
- Substance
- LEMON JUICE; ECHINACEA ANGUSTIFOLIA; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; LOBELIA INFLATA; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS LEAFY TWIG; ZINC GLUCONATE; THUJA OCCIDENTALIS LEAF; CAPSICUM; COPPER GLUCONATE; MANGANESE GLUCONATE; ARANEUS DIADEMATUS; ARSENIC TRIIODIDE; CENTAURIUM ERYTHRAEA FLOWER; CARPINUS BETULUS FLOWER; LARIX DECIDUA FLOWERING TOP; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; LACHESIS MUTA VENOM
- Active strength
- 1 [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
- 0000-00-00
- 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 | 43742-0236 | 43742-0236-1 | 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… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43742-0236-1 | 43742023601 | 60 mL in 1 BOTTLE, DROPPER (43742-0236-1) | 60 ml | 2015-12-10 | 2021-05-10 | No | No | Current |