GNAPHALIUM

FDA Drug Profile — GNAPHALIUM

GNAPHALIUM is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including GNAPHALIUM. Available dosage form: liquid.

Drug Details

Generic Name
GNAPHALIUM
Brand Names
GNAPHALIUM
Application Number
Sponsor
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
PSEUDOGNAPHALIUM OBTUSIFOLIUM

Indications and Usage

USES: May temporarily relieve minor symptoms of back and neck discomfort and sharp pain along the sciatic nerve, lower back and down the back of the legs.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: For external use only. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. When using this product • Do not get into eyes. Stop use and ask a doctor if • Conditions worsens • Symptoms last more than 7 days. Do not use if safety seal is broken or missing. unscented • non-greasy • no petroleum • no animal testing