Chamomilla
Chamomilla is an FDA drug label for the active ingredient CHAMOMILLA manufactured by Newton Laboratories, Inc. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230411.
- Generic name
- CHAMOMILLA
- Manufacturer
- Newton Laboratories, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 55714-9021
- Application
- N/A
- Label effective
- 20230411
Active ingredients
Indications & Usage
INDICATIONS & USAGE SECTION Teething pain; Diarrhea; Quarrelsome; Bad temper; Teething and colic
Dosage & Administration
DOSAGE & ADMINISTRATION SECTION Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) as needed or as directed by a health professional.
Contraindications
Not available.
Warnings
WARNINGS SECTION Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
Adverse Reactions
Not available.