United States · FDA National Drug Code directory
Nocturnal Enuresis Drops 2011
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
- 63083-2011_c58ac174-b51a-4fa1-a4cf-1325ec9abf90
- Product NDC
- 63083-2011
- Form
- LIQUID
- Composition / generic term
- Nocturnal Enuresis Drops
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 19840815
- Source listing expiry
- 20271231
Source-listed ingredients
- SUS SCROFA URINARY BLADDER — 6 [hp_X]/59mL
- THYROID, UNSPECIFIED — 6 [hp_X]/59mL
- CAUSTICUM — 12 [hp_X]/59mL
- EQUISETUM HYEMALE WHOLE — 12 [hp_X]/59mL
- FERROSOFERRIC PHOSPHATE — 12 [hp_X]/59mL
- WOOD CREOSOTE — 12 [hp_X]/59mL
- PULSATILLA MONTANA WHOLE — 12 [hp_X]/59mL
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE — 12 [hp_X]/59mL
These values do not establish equivalence or a dose recommendation.
Packages
- 59 mL in 1 BOTTLE, DROPPER (63083-2011-2) · 63083-2011-2
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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