Indications & Usage Section
Formulated for indigestion and stress.
Nux Vomica Pellet
FDA Label NDC 57556-016
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Historical Remedies for the product Nux Vomica (NDC 57556-016). 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.
Label Section Quick Index
Dosage & Administration Section
Directions: Dissolve under the tongue . Take every half hour as needed, or 4 times a day. Adults 4 pellets; Children (4-12 years) 2 pellets
Otc - Active Ingredient Section
1% Nux vomica 12x
Otc - Purpose Section
Formulated for indigestion and stress.
Inactive Ingredient Section
Inactive Ingredients: Organic beet-derived sucrose; gluten-free, lactose-free, non-GMO
Questions Section
Distributed by Historical Remedies; 122 S Wabasha, Saint Paul, MN 55107; 800-676-6654
www.historicalremedies.com
Warnings Section
Warning: Consult a doctor if symptoms persist more than 3 days or worsen. If pregnant or nursing, ask a doctor before use. Keep out of reach of children. Do not use if tamper-evident band is missing or broken.
Otc - Pregnancy Or Breast Feeding Section
If pregnant or breast-feeding, ask a doctor before use.
Otc - Keep Out Of Reach Of Children Section
Keep out of reach of children.
Package Label
Package Label (Hr Remedy Nux Vomica)
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