- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing consult a doctor before use. Avoid contact with eyes. Do not use if safety seals on box are broken or missing. BEST WHEN USED WITHIN 30 DAYS OF OPENING.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CALENDULA THUJA
calendula thuja gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3204 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP 2 [hp_X] in 1 g ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED 2 [hp_X] in 1 g ORIGANUM MAJORANA WHOLE (UNII: R40XM3HU5X) (ORIGANUM MAJORANA WHOLE - UNII:R40XM3HU5X) ORIGANUM MAJORANA WHOLE 2 [hp_X] in 1 g LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (LILIUM LANCIFOLIUM WHOLE FLOWERING - UNII:X67Z2963PI) LILIUM LANCIFOLIUM WHOLE FLOWERING 3 [hp_X] in 1 g THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (THUJA OCCIDENTALIS WHOLE - UNII:5HBV6WCE3N) THUJA OCCIDENTALIS WHOLE 3 [hp_X] in 1 g WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE 6 [hp_X] in 1 g PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 6 [hp_X] in 1 g SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 7 [hp_X] in 1 g CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 33 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength CITRUS PARADISI SEED (UNII: 12F08874Y7) TEA TREE OIL (UNII: VIF565UC2G) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM ALGINATE (UNII: C269C4G2ZQ) LACTIC ACID (UNII: 33X04XA5AT) EUCALYPTUS OIL (UNII: 2R04ONI662) ROSEMARY OIL (UNII: 8LGU7VM393) SAGE OIL (UNII: U27K0H1H2O) THYME OIL (UNII: 2UK410MY6B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-3204-8 120 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product 09/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-3204)