Label: EPSOM SALT- magnesium sulfate granule
- NDC Code(s): 0363-0395-01, 0363-0395-03, 0363-0395-04, 0363-0395-06
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 4, 2022
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)
- Active ingredient
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- kidney disease
- a magnesium restricted diet
- stomach pain, nausea or vomiting
- noticed a sudden change in bowel habits that lasts more than 2 weeks
-
Directions
- do not exceed more than 2 doses per day; if necessary repeat dosage in 4 hours
age dose adults and children 12 years and older 2-4 level teaspoons dissolved in a full glass (8oz) of water children 6 to 11 years 1-2 level teaspoons dissolved in a full glass (8oz) of water
Not recommended for children under 6 years of age. - Other information
- Inactive ingredient
- Questions or comments?
- Principal Display Panel
- Package Label
-
INGREDIENTS AND APPEARANCE
EPSOM SALT
magnesium sulfate granuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0395 Route of Administration ORAL, TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE 1 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0395-04 1810 g in 1 POUCH; Type 0: Not a Combination Product 04/30/2016 2 NDC:0363-0395-06 2721 g in 1 POUCH; Type 0: Not a Combination Product 04/30/2016 3 NDC:0363-0395-03 1360 g in 1 POUCH; Type 0: Not a Combination Product 04/30/2016 4 NDC:0363-0395-01 454 g in 1 POUCH; Type 0: Not a Combination Product 04/30/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 04/30/2016 Labeler - Walgreens (008965063)