Label: EQUATE MUSCLE CRAMP AND SPASM RELIEF- magnesium sulfate heptahydrate liquid
- NDC Code(s): 79903-100-18
- Packager: Walmart, 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 December 31, 2023
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Inactive Ingredients
Inactive ingredients
Aloe vera leaf juice, Ascorbic acid, Caprylyl glycol, Citric acid, Cocamidopropyl betaine, Disodium laureth sulfosuccinate, Ethanol, Glycerin, Ionic colloidal silver, Methyl gluceth-10, PEG-8 Dimethicone, PEG-14, PEG-33, Phenoxyethanol, Potassium sorbate, Purified water, Sodium benzoate, Sodium bicarbonate, Sodium cocoyl isethionate, Sorbic acid, Tocopherols (soy)
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INGREDIENTS AND APPEARANCE
EQUATE MUSCLE CRAMP AND SPASM RELIEF
magnesium sulfate heptahydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-100 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 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ALOE VERA LEAF (UNII: ZY81Z83H0X) SILVER (UNII: 3M4G523W1G) GLYCERIN (UNII: PDC6A3C0OX) ASCORBIC ACID (UNII: PQ6CK8PD0R) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) TOCOPHEROL (UNII: R0ZB2556P8) PEG-8 DIMETHICONE (UNII: GIA7T764OD) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ALCOHOL (UNII: 3K9958V90M) METHYL GLUCETH-10 (UNII: N0MWT4C7WH) POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A) SORBIC ACID (UNII: X045WJ989B) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-100-18 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/19/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/19/2022 Labeler - Walmart, inc (051957769)