Male Vitality
- Product NDC
- 71742-0015
- Requested package NDC
- 71742-0015-1
- 11-digit product format
- 717420015
- Labeler code
- 71742
- Product ID
- 71742-0015_de1c8831-eec6-4729-b35f-8c9e1f740f84
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Damiana, Korean Ginseng, Populus Tremuloides, Nuphar Luteum, Arnica Montana, Carduus Marianus, Galium Aparine, Lactuca Virosa, Caladium Seguinum, Hepar Suis, Orchitinum (Suis), Thymus (Suis), Glandula Suprarenalis Suis, Hypophysis Suis, Thyroidinum (Suis), Testosterone, Phosphoricum Acidum, Thuja Occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Guangzhou Renuma Medical Systems Co., Ltd
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-10-31
- Marketing end
- 0000-00-00
- Substance
- TURNERA DIFFUSA LEAFY TWIG; ASIAN GINSENG; POPULUS TREMULOIDES BARK; NUPHAR LUTEA ROOT; ARNICA MONTANA WHOLE; MILK THISTLE; GALIUM APARINE WHOLE; LACTUCA VIROSA WHOLE; DIEFFENBACHIA SEGUINE WHOLE; PORK LIVER; SUS SCROFA TESTICLE; SUS SCROFA THYMUS; SUS SCROFA ADRENAL GLAND; SUS SCROFA PITUITARY GLAND; THYROID, PORCINE; TESTOSTERONE; PHOSPHORIC ACID; THUJA OCCIDENTALIS LEAFY TWIG
- 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_C]/mL; [hp_C]/mL
- DEA schedule
- CIII
- 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 | 71742-0015 | 71742-0015-1 | 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… |
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 |
|---|---|---|---|---|---|---|---|---|
| 71742-0015-1 | 71742001501 | 59 mL in 1 PACKAGE (71742-0015-1) | 59 ml | 2017-10-31 | 0000-00-00 | No | No | Current |