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Pill Identifier Information of DOSS Sodium 100 MG Oral Capsule

Drug Information

DOSS Sodium 100 MG Oral Capsule

Imprint: A92
Shape: C48345
Color: C48326
Ingredients: Docusate
Size: 14.00
Score: 1
Rxtty: SY
Author: Rebel Distributors Corp
Inactive Ingredients: CITRIC ACID MONOHYDRATE / D&C RED NO. 33 / D&C YELLOW NO. 10 / ETHYL VANILLIN / FD&C BLUE NO. 1 / FD&C RED NO. 40 / FD&C YELLOW NO. 6 / GELATIN / GLYCERIN / MANNITOL / METHYLPARABEN / POLYETHYLENE GLYCOL / PROPYLENE GLYCOL / PROPYLPARABEN / SORBITOL / WATER>

Complete Information

  • Active ingredient

    Docusate Sodium 100mg

  • Purpose

    Stool Softener

  • Keep Out of Reach of Children

    In case of overdose, get medical help or contact a Poison Control center right way.

  • Uses

    Prevents / relieves dry hard stool. Results usually occur 1 to 3 days after the first dose.

  • Warnings

    Do not use for more than one week unless directed by a doctor.

    Ask a doctor before use if you have abdominal pain, nausea, or vomiting; have noticed a sudden change in bowel habits that lasts over 2 weeks,; are taking mineral oil.

    Stop use and ask a doctor if you have no bowel movement within 3 days; you have rectal bleeding. These could be signs of a serious condition.

    If pregnant or breast-feeding, ask a health professional before use.

    Tamper Evident: Do not use if imprinted seal under cap is missing or broken.

  • Directions

    Adults and children 12 years and older: take 1-2 softgels daily until first bowel movement; 1 softgel daily thereafter, or as directed by a doctor.

    Children under 12: consult a doctor.

    Do not exceed recommended dose.

  • Other Information

    Each softgel contains sodium 5mg.

    Product from Canada or USA

    Store at room temperature, 15°C-30°C (59°F-86°F)

  • Inactive ingredients

    may contain cirtic acid, D&C red no. 33, D&C yellow no. 10, ethyl vanillin, FD&C blue no. 1, FD&C re no. 40 FD&C yellow no. 6, gelatin, glycerin, edible ink, mannitol, methylparaben, polyethylene glycol, propylene glycol, propylparaben, sorbitol, water.

    Distributed by:

    Geri-Care Pharmaceuticals Corp.

    Brooklyn, NY 11204

    Repackaged by:

    Rebel Distributors Corp

    Thousand Oaks, CA 91320

  • Package/Label Principal Display Panel

    Docusate Sodium 100mg

  • INGREDIENTS AND APPEARANCE
    DOCUSATE SODIUM 
    docusate sodium capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21695-590(NDC:57896-401)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM100 mg
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    ETHYL VANILLIN (UNII: YC9ST449YJ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GELATIN (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MANNITOL (UNII: 3OWL53L36A)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorREDScoreno score
    ShapeOVALSize14mm
    FlavorImprint Code A92
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21695-590-2020 in 1 BOTTLE
    2NDC:21695-590-3030 in 1 BOTTLE
    3NDC:21695-590-9090 in 1 BOTTLE
    4NDC:21695-590-00100 in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33401/01/2007
    Labeler - Rebel Distributors Corp (118802834)
    Establishment
    NameAddressID/FEIBusiness Operations
    Rebel Distributors Corp118802834RELABEL, REPACK