United States · FDA National Drug Code directory
Teething
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
- 43857-0406_f00e158b-3a49-4114-a9aa-738ce56d74ad
- Product NDC
- 43857-0406
- Form
- LIQUID
- Composition / generic term
- Arnica Montana, Trifolium Pratense, Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Chamomilla, Kreosotum, Silicea
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20160727
- Source listing expiry
- 20261231
Source-listed ingredients
- ARNICA MONTANA — 3 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER — 3 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/mL
- CALCIUM FLUORIDE — 12 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE — 12 [hp_X]/mL
- MATRICARIA RECUTITA — 12 [hp_X]/mL
- WOOD CREOSOTE — 12 [hp_X]/mL
- SILICON DIOXIDE — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (43857-0406-1) · 43857-0406-1
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →