GLUCOREKT
- Product NDC
- 59469-137
- 11-digit product format
- 594690137
- Labeler code
- 59469
- Product ID
- 59469-137_9c83fe87-216c-43f6-b3ae-84b86f857845
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LACTIC ACID, DL-, SULFURIC ACID, ONION, CHIONANTHUS VIRGINICUS BARK, PHOSPHORUS, ZINC SULFATE HEPTAHYDRATE, CORN SILK, and SYZYGIUM CUMINI FRUIT
- Dosage form
- SOLUTION/ DROPS
- Route
- ORAL
- Labeler
- PEKANA Naturheilmittel GmbH
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2008-12-11
- Marketing end
- 0000-00-00
- Substance
- LACTIC ACID, DL-; SULFURIC ACID; ONION; CHIONANTHUS VIRGINICUS BARK; PHOSPHORUS; ZINC SULFATE HEPTAHYDRATE; CORN SILK; SYZYGIUM CUMINI FRUIT
- Active strength
- 6 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; mg/50mL; mg/50mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record