Active Ingredients
Aconitum napellus 12C, Hypericum perforatum 12C, Lycopodium clavatum 12C, Phosphorus 12C, Rhus toxicodendron 12C, Secale cornutum 12C
Neuragen
FDA Label NDC 15377-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Origin Biomed Inc. for the product Neuragen (NDC 15377-010). 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 active ingredients, purpose, uses, warnings, otc - pregnancy or breast feeding, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical analgesic
Uses
For rapid, temporary relief from pain described as shooting, burning, tingling and stabbing pain, especially in the hands and feet.
Warnings
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Otc - Pregnancy Or Breast Feeding
Do not use if pregnant or breastfeeding.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Apply cream to the affected area up to 4 times daily.
Other Information
Store at room temperature 59-86 degrees F (15-30 degrees C). Do not use if tamper seal is broken.
Inactive Ingredients
water, bergamot oil, eucalyptus oil, geranium oil, geraniol, lavender oil, tea tree oil, geraniol, propylene glycol, poloxamer 407, sodium benzoate, benzoic-acid, and ethyl alcohol
Questions?
Call 1-902-423-5745 www.neuragen.com |
Package Label.Principal Display Panel
Pain Relief Cream Fast acting relief from
 Neuragen Cream Carton (Neuragencreamcarton) |
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