EPSOM SALT- epsom salt granule 
P & L Development, LLC

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Drug Facts

Active ingredient

Magnesium sulfate USP 100%

Purpose

 Saline laxative

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

Ask a doctor or pharmacist before use if you are

 presently taking a prescription drug.

When using this product

  • do not use more than directed

Stop use and ask a doctor if

  • you have rectal bleeding or failure to have a bowel movement after use. This may indicate a serious condition.
  • you need to use a laxative for more than 1 week

If pregnancy or breast-feeding,

 ask a health professional before use.

Keep out of reach of children.

 In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

agedose
 adults and children 12  years and older2-4 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

none 

Questions or comments?

For laxative or soak, call 1-877-753-3935 Monday- Friday 9AM-5PM EST

Principal Display Panel

EPSOM SALTS

MAGNESIUM SULFATE

SALINE LAXATIVE

Net Wt LB (kg)

TAMPER EVIDENT: DO NOT USE IF HEAT SEALED POUCH IS IMPROPERLY SEALED.

Distributed by:

PL Developments, 1874 Hwy 72 W

Clinton, SC 29325

Package Label

Magnesium Sulfate USP 100%

WHITE MOUNTAIN Epsom Salt

EPSOM SALT 
epsom salt granule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49580-0394
Route of AdministrationORAL, TOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE, UNSPECIFIED1 g  in 1 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49580-0394-41814 g in 1 POUCH; Type 0: Not a Combination Product12/31/2017
2NDC:49580-0394-1454 g in 1 POUCH; Type 0: Not a Combination Product12/31/2017
3NDC:49580-0394-2907 g in 1 POUCH; Type 0: Not a Combination Product12/31/2017
4NDC:49580-0394-83628 g in 1 POUCH; Type 0: Not a Combination Product12/31/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00712/31/2017
Labeler - P & L Development, LLC (101896231)

Revised: 4/2024
Document Id: 12b43673-3251-49aa-a76e-998d24a3beb2
Set id: a343bb9f-0b63-4464-99a0-f7137cd2125a
Version: 8
Effective Time: 20240415
 
P & L Development, LLC