EPSOM SALTS RELIEF- magnesium sulfate heptahydrate granule 
Blue Cross Laboratories, Inc.

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.


Relief  Epsom Salt

Active Ingredients Purpose

Magnesium Sulfate [heptahydrate]100% Saline Laxative

-For relief of occasional constipation (irregularity)

-this product generally produces bowel movement in 1/2 to 6 hours

Keep out of reach of children

-For relief of occasional constipation (irregularity)

-this product generally produces bowel movement in 1/2 to 6 hours


Ask a doctor is you have

- kidney disease

- a magnesium restricted diet

- abdominal pain, nausea, or vomiting

- noticed a sudden change in bowel habits that persists over a period of 2 weeks

- already used a laxative for a period longer than 1 week

Ask a doctor of pharmacist before use if you are taking any other drug. Take this product 2 or more hours before or after other drugs. Laxatives may affect how other drugs work.

If pregnant or breast-feeding, as a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.


-do not exceed more than 2 doses per day

-drink a full glass (8 ounces) of liquid with each dose

-dissolve the dose in 8 ounces of water. Lemon juice may be added to improve the taste.

-adults and children 12 years and over: 2 to 4 level teaspoons (10 to 20 grams) daily

-children 6 to under 12 years: 1 to 2 level teaspoons (5 to 10 grams) daily

-children under 6 years: consult a doctor

Other information

Magnesium content: 495 mg per teaspoon


Epsom Salt

Magnesium Sulfate

A Soaking aid for minor sprains & bruises

Use as a saline laxative

NET WT 16 Oz (1 LB) 454 g

image of back label

image of front label

magnesium sulfate heptahydrate granule
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:22431-124
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:22431-124-01 1810 g in 1 BAG
2 NDC:22431-124-02 454 g in 1 BAG
3 NDC:22431-124-03 454 g in 1 CARTON
4 NDC:22431-124-04 907 g in 1 BAG
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part334 07/09/2010
Labeler - Blue Cross Laboratories, Inc. (008298879)
Registrant - Blue Cross Laboratories, Inc. (008298879)
Name Address ID/FEI Business Operations
Hefei Yatai Daily Chemical Products Co., Ltd. 654641724 manufacture(22431-124)

Revised: 1/2014
Document Id: 75508b77-da85-4f33-b2a9-07c1b401e000
Set id: d4937f2c-095d-40ca-94e7-6d88df95768e
Version: 12
Effective Time: 20140129
Blue Cross Laboratories, Inc.