Active Ingredients
GRAPHITES 6C
SEPIA 6C
SULPHUR 6C
THUJA 6C
Fungus
FDA Label NDC 68428-009
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 Fungus (NDC 68428-009). 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, uses, keep out of reach of children, indications, stop use and ask doctor, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
To relieve the symptoms of burning and itching eruptions of the skin, as in ringworm or athlete’s foot.
Keep Out Of Reach Of Children
Keep this and all medicines out of reach of children.
Indications
Indications:
GRAPHITES Cracks in skin
SEPIA Indifference
SULPHUR Skin problems
THUJA Warts
Stop Use And Ask Doctor
If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.
Directions
Adults 2 pellets every 3 hours for 2 days. Then 2 pellets morning and night for 2 weeks.
Children: 1 pellet. Repeat as necessary.
Inactive Ingredients
Sucrose/Lactose
Principal Display Panel
Image Of Bottle Label (Fungus)
* Please review the disclaimer below.
