Home > Pill Identifier > DOSS Sodium 250 MG Oral Capsule

Pill Identifier Information of DOSS Sodium 250 MG Oral Capsule

Drug Information

DOSS Sodium 250 MG Oral Capsule

Imprint: NV12
Shape: C48345
Color: C48326
Ingredients: Docusate
Size: 20.00
Score: 1
Rxtty: SY
Author: National Vitamin Company
Inactive Ingredients: FD&C RED NO. 40 / FD&C YELLOW NO. 6 / GELATIN / GLYCERIN / POLYETHYLENE GLYCOL 1000 / PROPYLENE GLYCOL / WATER / SORBITOL>

Complete Information

  • Active Ingredient (in each softgel)

    Docusate Sodium 250 mg

  • Purpose

    Stool Softener

  • Uses

    •
    For the relief of occasional constipation.
    •
    Helps to prevent dry, hard stools.
    •
    This product generally produces a bowel movement within 12 to 72 hours.
  • WARNINGS Do not use:

    •
    If you are currently taking mineral oil, unless directed by a doctor.
    •
    When abdominal pain, nausea, or vomiting are present.
    •
    For longer than one week unless directed by a doctor.

    Ask a doctor before use

    if you notice a sudden change in bowel habits that persists over a period of two weeks.

    Stop use and ask a doctor

    if you have rectal bleeding or you fail to have a bowel movement after use.

    If pregnant or breast-feeding,

    ask a healthcare professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and Children over 12 years of age

    Take orally 1 softgel preferably at bedtime for
    2-3 days or until bowel movements are normal, or as directed by a doctor.

    Children under 12 years of age

    Do not use this product for children under 12 years of age, unless directed by a doctor.

  • Other Information

    •
    Each softgel contains 13 mg of Sodium.
    •
    Store at room temperature between 15°C to 30°C (59°F to 86°F).
    •
    Do not use if printed seal under cap is broken or missing.
    •
    For identification purposes, each softgel will have an imprint that reads NV12.
  • Inactive Ingredients

    FD&C Red #40, FD&C Yellow #6, Gelatin, Glycerin, Ink (Edible), Polyethylene Glycol, Propylene Glycol, Purified Water, Sorbitol.

  • Questions

    Call 1 (800) 682-9862

  • Package/Label Principal Display Panel

    NDC 54629-601-01
    Life-Line®
    Docusate Sodium, USP
    Stool Softener
    250 mg Each
    100 Softgels

    Manufactured and Distributed by
    National Vitamin Company
    Casa Grande, AZ 85122

    Bottle Label

    Bottle Label

  • INGREDIENTS AND APPEARANCE
    DOCUSATE SODIUM 
    docusate sodium capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54629-601
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM250 mg
    Inactive Ingredients
    Ingredient NameStrength
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorREDScoreno score
    ShapeOVALSize20mm
    FlavorImprint Code NV12
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54629-601-01100 in 1 BOTTLE; Type 0: Not a Combination Product05/01/200010/31/2027
    2NDC:54629-601-991000 in 1 BOTTLE; Type 0: Not a Combination Product05/01/200010/31/2027
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00705/01/200010/31/2027
    Labeler - National Vitamin Company (102098324)
    Establishment
    NameAddressID/FEIBusiness Operations
    National Vitamin Company102098324MANUFACTURE(54629-601)