Label: CVS FOAMING MUSCLE RELIEF- magnesium sulfate heptahydrate liquid
- NDC Code(s): 59779-541-05
- Packager: CVS Health
- Category: HUMAN OTC 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 11, 2024
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INGREDIENTS AND APPEARANCE
CVS FOAMING MUSCLE RELIEF
magnesium sulfate heptahydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-541 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 506 mL Inactive Ingredients Ingredient Name Strength COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) WATER (UNII: 059QF0KO0R) PEG/PPG-20/15 DIMETHICONE (UNII: 06R6X77P9C) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ALOE VERA LEAF (UNII: ZY81Z83H0X) PHENOXYETHANOL (UNII: HIE492ZZ3T) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-541-05 210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/06/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/06/2022 Labeler - CVS Health (062312574)