United States · FDA National Drug Code directory
DNA Insulin Drops 2019
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
- 63083-2019_91ade3ff-25ab-464b-8084-9fb5d5d6d955
- Product NDC
- 63083-2019
- Form
- LIQUID
- Composition / generic term
- DNA Insulin Drops
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 19840815
- Source listing expiry
- 20271231
Source-listed ingredients
- CHROMIUM — 6 [hp_X]/59mL
- LYCOPODIUM CLAVATUM SPORE — 6 [hp_X]/59mL
- VANADIUM — 6 [hp_X]/59mL
- PANCRELIPASE AMYLASE — 6 [hp_X]/59mL
- INSULIN GLULISINE — 12 [hp_X]/59mL
- PHOSPHORIC ACID — 30 [hp_X]/59mL
- URANYL NITRATE HEXAHYDRATE — 30 [hp_X]/59mL
- RADIUM BROMIDE — 60 [hp_X]/59mL
These values do not establish equivalence or a dose recommendation.
Packages
- 59 mL in 1 BOTTLE, DROPPER (63083-2019-2) · 63083-2019-2
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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