Label: THERAWORX RELIEF MUSCLE CRAMP AND SPASM RELIEF aerosol, foam
-
Contains inactivated NDC Code(s)
NDC Code(s): 71064-0003-0 - Packager: Relion Manufacturing
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 December 7, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INSTRUCTIONS FOR USE
- 0003 Bottle Label
-
INGREDIENTS AND APPEARANCE
THERAWORX RELIEF MUSCLE CRAMP AND SPASM RELIEF
theraworx relief muscle cramp and spasm relief aerosol, foamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71064-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71064-0003-0 1 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/22/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/22/2017 Labeler - Relion Manufacturing (085629765) Registrant - Avadim Technologies Inc. (041443877) Establishment Name Address ID/FEI Business Operations Relion Manufacturing 085629765 manufacture(71064-0003)
