Label: FUNGUS FREE- sambucus nigra flower, calendula officinalis flower, thuja occidentalis leafy twig, echinacea angustifolia salve
- NDC Code(s): 52810-511-11
- Packager: PUREMEDY
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated January 11, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FUNGUS FREE
sambucus nigra flower, calendula officinalis flower, thuja occidentalis leafy twig, echinacea angustifolia salveProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52810-511 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T) (SAMBUCUS NIGRA FLOWER - UNII:07V4DX094T) SAMBUCUS NIGRA FLOWER 1 [hp_X] in 100 mL CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (CALENDULA OFFICINALIS FLOWER - UNII:P0M7O4Y7YD) CALENDULA OFFICINALIS FLOWER 1 [hp_X] in 100 mL THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 1 [hp_X] in 100 mL ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA 1 [hp_X] in 100 mL Inactive Ingredients Ingredient Name Strength OLIVE OIL (UNII: 6UYK2W1W1E) SAFFLOWER OIL (UNII: 65UEH262IS) YELLOW WAX (UNII: 2ZA36H0S2V) CANADA BALSAM (UNII: K304VI98I3) PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y) OREGANO LEAF OIL (UNII: 7D0CGR40U1) TEA TREE OIL (UNII: VIF565UC2G) AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52810-511-11 30 mL in 1 JAR; Type 0: Not a Combination Product 10/18/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/18/2012 Labeler - PUREMEDY (003552251) Establishment Name Address ID/FEI Business Operations PUREMEDY 003552251 manufacture(52810-511)