Label: THERAWORX JOINT RELIEF ROLL ON- frankincense liquid
- NDC Code(s): 61594-027-00
- Packager: AVADIM HOLDINGS, INC.
- 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 August 31, 2023
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- Drug Facts
- Active Ingredient
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Inactive Ingredients (Alphabetical)
Allantoin, Aloe barbadensis Leaf Extract, Aloe barbadensis Leaf Juice, Aqua (Water), Benzyl Alcohol, Calcium Carbonate, Citric Acid, Cocamidopropyl Betaine, Colloidal Silver, Croton Lechieri Resin Extract, Decyl Glucoside, Ethylhexylglycerin, Glycerin, PEG/PPG-4/12 Dimethicone, Parfum (Fragrance), Potassium Sorbate, Sodium Benzoate, Tetrasodium EDTA, Tocopherol Acetate, Vitex Agnus- Castus Extract, Xanthan Gum, Yeast Extract, Yucca shidigera Extract
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INGREDIENTS AND APPEARANCE
THERAWORX JOINT RELIEF ROLL ON
frankincense liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61594-027 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FRANKINCENSE (UNII: R9XLF1R1WM) (FRANKINCENSE - UNII:R9XLF1R1WM) FRANKINCENSE 8 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) BENZYL ALCOHOL (UNII: LKG8494WBH) CALCIUM CARBONATE (UNII: H0G9379FGK) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SILVER (UNII: 3M4G523W1G) CROTON LECHLERI RESIN (UNII: GGG6W25C63) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-4/12 DIMETHICONE (UNII: JAN3585W85) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CHASTE TREE FRUIT (UNII: 433OSF3U8A) XANTHAN GUM (UNII: TTV12P4NEE) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) YUCCA SCHIDIGERA WHOLE (UNII: 08A0YG3VIC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61594-027-00 1 in 1 CARTON 01/15/2023 1 74 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/15/2023 Labeler - AVADIM HOLDINGS, INC. (118512488)