Label: THERAWORX NERVE RELIEF FOAM- onion, hypericum perforatum whole, sanguinaria canadensis root aerosol, foam
- NDC Code(s): 61594-020-00
- 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 April 25, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
- Directions
-
Inactive Ingredients (Alphabetical)
Allantoin, Aloe Barbadensis Leaf Extract, Aloe Barbadensis Leaf Juice, Aqua (Water), Citric Acid, Cocamidopropyl Betaine, Colloidal Silver, Croton Lechieri Resin Extract, Decyl Glucoside, Diazolidinyl Urea, Glycerin, Leuconostoc/ Radish Root Ferment Filtrate, Methylparaben, PEG / PPG - 4/12 Dimethicone, Propylene Glycol, Propylparaben, Tetrasodium EDTA, Tocopheryl Acetate, Yeast Extract
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
THERAWORX NERVE RELIEF FOAM
onion, hypericum perforatum whole, sanguinaria canadensis root aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61594-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 10 [hp_X] in 1 mL HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM WHOLE 10 [hp_X] in 1 mL SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508) SANGUINARIA CANADENSIS ROOT 8 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ALLANTOIN (UNII: 344S277G0Z) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SILVER (UNII: 3M4G523W1G) CROTON LECHLERI RESIN (UNII: GGG6W25C63) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) GLYCERIN (UNII: PDC6A3C0OX) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) METHYLPARABEN (UNII: A2I8C7HI9T) PEG/PPG-4/12 DIMETHICONE (UNII: JAN3585W85) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61594-020-00 210 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/01/2022 Labeler - AVADIM HOLDINGS, INC. (118512488) Registrant - AVADIM HOLDINGS, INC. (118512488) Establishment Name Address ID/FEI Business Operations AVADIM HOLDINGS, INC. 118512488 manufacture(61594-020)