Indications & Usage Section
Aggravation from motion or movement; back pain and stiffness; muscle aches and pain, joint pain and swelling.
The following Structured Product Label (SPL) was submitted to the FDA by Newton Laboratories, Inc. for the product Bryonia (NDC 55714-9019). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage section, dosage & administration section, otc - active ingredient section, otc - purpose section, inactive ingredient section, questions section, warnings section, otc - pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Aggravation from motion or movement; back pain and stiffness; muscle aches and pain, joint pain and swelling.
Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) at bedtime or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.
Bryonia 10x
Aggravation from motion or movement; back pain and stiffness; muscle aches and pain; joint pain and swelling.
Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.
newtonlabs.net – Questions? 800.448.7256
Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013
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.
If pregnant or breast-feeding, ask a doctor before use.
Keep out of reach of children.
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