United States · FDA National Drug Code directory
RET Gallbladder 7007
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63083-7007_b82992bf-fb5e-4189-8bc5-531d8268b0b1
- Product NDC
- 63083-7007
- Form
- LIQUID
- Composition / generic term
- RET Gallbladder
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 19840815
- Source listing expiry
- 20271231
Source-listed ingredients
- ULEX EUROPAEUS FLOWER — 3 [hp_X]/29.5mL
- ELEUTHEROCOCCUS SENTICOSUS ROOT OIL — 3 [hp_X]/29.5mL
- SALIX ALBA FLOWERING TOP — 3 [hp_X]/29.5mL
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM — 3 [hp_X]/29.5mL
- COPPER — 30 [hp_X]/29.5mL
- LACHESIS MUTA VENOM — 30 [hp_X]/29.5mL
- LYCOPODIUM CLAVATUM SPORE — 30 [hp_X]/29.5mL
- SODIUM CHLORIDE — 30 [hp_X]/29.5mL
- DATURA STRAMONIUM — 30 [hp_X]/29.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 29.5 mL in 1 BOTTLE, DROPPER (63083-7007-1) · 63083-7007-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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