Glucose Control T015
Active substance: SYZYGIUM CUMINI SEED, SUS SCROFA ADRENAL GLAND, GOLDENSEAL, SUS SCROFA PITUITARY GLAND, SUS SCROFA PANCREAS, KIDNEY BEAN, ACETIC ACID, LACTIC ACID, PHOSPHORIC ACID, PHOSPHORUS, URANYL NITRATE HEXAHYDRATE
LIQUID · SYZYGIUM CUMINI SEED 3 [hp_X]/mL, SUS SCROFA ADRENAL GLAND 6 [hp_X]/mL, GOLDENSEAL 6 [hp_X]/mL, SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL, SUS SCROFA PANCREAS 6 [hp_X]/mL, KIDNEY BEAN 9 [hp_X]/mL, ACETIC ACID 12 [hp_X]/mL, LACTIC ACID 12 [hp_X]/mL, PHOSPHORIC ACID 12 [hp_X]/mL, PHOSPHORUS 12 [hp_X]/mL, URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL
United StatesActive
Marketing holder: Guangzhou Renuma Medical Systems Co., Ltd
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
- SYZYGIUM CUMINI SEED · 3 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND · 6 [hp_X]/mL
- GOLDENSEAL · 6 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND · 6 [hp_X]/mL
- SUS SCROFA PANCREAS · 6 [hp_X]/mL
- KIDNEY BEAN · 9 [hp_X]/mL
- ACETIC ACID · 12 [hp_X]/mL
- LACTIC ACID · 12 [hp_X]/mL
- PHOSPHORIC ACID · 12 [hp_X]/mL
- PHOSPHORUS · 12 [hp_X]/mL
- URANYL NITRATE HEXAHYDRATE · 12 [hp_X]/mL
Showing products with this active substance, combinations included; the full composition is shown for each product.
| Country | Products |
|---|---|
| RU 3 |
|
- Registration number
- 71742-0009
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
- product · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.9 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source
- ingredients.10 · openFDA NDC · 71742-0009 · Verified 2026-10-09 · open in source