Otc - Active Ingredient
GRAPHITE
Graphites Pellet
FDA Label NDC 71919-826
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Washington Homeopathic Products for the product Graphites (NDC 71919-826). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Indicated for cracks in skin
Otc - Keep Out Of Reach Of Children
As with all medicines, keep out of reach of children.
Indications & Usage
Graphites Cracks in skin
Warnings
If symptoms worsen or persist for more than 7 days, or if pregnant or nursing, consult a licensed practitioner.
Dosage & Administration
Directions: Adults & children: Dissolve 4 pellets under the tongue 3 times a day or as directed by a licensed practitioner. Other information: Do not use if seal is broken.
Inactive Ingredient
SUCROSE/LACTOSE
Package Label.Principal Display Panel
The OTC potency range of Graphites is 30c - 200c
Availability is subject to change.
Graphites (Graphites)
* Please review the disclaimer below.
