OTC - ACTIVE INGREDIENT SECTION
Active ingredient: Ginsenoside Compound K 50 mg/ 10 g
Tuberculosis Eliminator
- Manufacturer
- Hainan Zehuitang Biotechnology Co., LTD
- Effective date
- 2025-02-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:55:47
Label at a glance#
ProductTuberculosis Eliminator
Active ingredientGINSENOSIDE COMPOUND K
Label structure15 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Purpose: Regulate the human immune system; Treat tuberculosis
WARNINGS SECTION
Warnings:
Do not use if you are allergic to this product and its ingredients
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
Other diseases;
Or take some medicines
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are Pregnant women Or infants
OTC - WHEN USING SECTION
When using this product:
Take before meals,
Take it half an hour before going to bed
OTC - STOP USE SECTION
Stop use and ask a doctor if There was no sign of relief after taking for 4 weeks.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions:
Take one bottle orally with water, three times daily.
For internal use only.
INACTIVE INGREDIENT SECTION
Inactive ingredients: CORN STAREH, YEAST. BETA. -D-GLUCAN, URSOLIC ACID
OTC - QUESTIONS SECTION
Questions? 123-555-1234
STATEMENT OF IDENTITY SECTION
Other information:
Store at 5-30℃,
Keep out of direct sunlight
INDICATIONS & USAGE SECTION
Use: Regulate the human immune system; Treat tuberculosis
When using this productTake before mealsTake it half an hour before going to bed
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84428-103-01 | Tuberculosis Eliminator | 50 g in 1 BOTTLE | GRANULE | 50 | 1 | |
| 84428-103-02 | Tuberculosis Eliminator | 7 in 1 BOX | GRANULE | 7 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Tuberculosis Eliminator
- Ginsenoside Compound K
- YEAST .BETA.-D-GLUCAN
- STARCH, CORN
- URSOLIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84428-103 | 84428-103-01, 84428-103-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| YEAST .BETA.-D-GLUCAN | 44FQ49X6UN | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| URSOLIC ACID | P3M2575F3F | IACT |
| GINSENOSIDE COMPOUND K | G8D4792Q7K | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 2eb5926c-e9dd-59f9-e063-6294a90aae44 | 2eb59817-cf1f-4b22-e063-6394a90a05db | 2025-02-22 | Warnings | 2eb5926c-e9dd-59f9-e063-6294a90aae44 2eb59817-cf1f-4b22-e063-6394a90a05db |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.