United States · FDA National Drug Code directory
Teething Drops 2120
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
- 63083-2120_f97c3e15-b5fe-476d-9cb4-4d565dd902d0
- Product NDC
- 63083-2120
- Form
- LIQUID
- Composition / generic term
- Teething Drops
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 19840815
- Source listing expiry
- 20271231
Source-listed ingredients
- EUGENOL — 3 [hp_X]/59mL
- ULMUS RUBRA BARK — 3 [hp_X]/59mL
- ARTEMISIA ANNUA FLOWERING TOP — 3 [hp_X]/59mL
- MENTHA X PIPERITA WHOLE — 4 [hp_X]/59mL
- CLEMATIS RECTA FLOWERING TOP — 6 [hp_X]/59mL
- CITRULLUS COLOCYNTHIS FRUIT PULP — 6 [hp_X]/59mL
- COPPER — 6 [hp_X]/59mL
- MYRRH — 6 [hp_X]/59mL
- BRYONIA ALBA ROOT — 12 [hp_X]/59mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/59mL
These values do not establish equivalence or a dose recommendation.
Packages
- 59 mL in 1 BOTTLE, DROPPER (63083-2120-2) · 63083-2120-2
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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