FDA.reportPublic FDA data

Konsyl Orange Daily Fiber

Manufacturer
Konsyl Pharmaceuticals, Inc.
Effective date
2021-12-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:20:16

Label at a glance#

ProductKonsyl Orange Daily Fiber
Active ingredientPSYLLIUM HUSK
Label structure9 sections

Dosage and administration

Mix this product with at least 8 ounces (a full glass) of water or other fluid. Taking this product without enough fluid may cause choking. See choking warning.  adults and children 12 years and older  one teaspoon 1 to 3 times daily  children 6 to under 12 years of age  1/2 teaspoon 1 to 3 times daily  children under 6 years of age  consult a doctor

Label contents#

Full prescribing information#

Active Ingredient (in each teaspoon)

OTC - ACTIVE INGREDIENT SECTION

Psyllium Hydrophilic Mucilloid 3.4g

Purpose

OTC - PURPOSE SECTION

Bulk-forming laxative

Use

INDICATIONS & USAGE SECTION

For relief of occasional constipation and aid in regularity. This product generally produces bowel movements within 12-72 hours.

Warnings

WARNINGS SECTION

Choking Taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking. Do not take this product if you have difficulty in swallowing. If you experience chest pain, vomiting or difficulty in swallowing or breathing after taking this product, seek immediate medical attention.

Do not use

OTC - DO NOT USE SECTION

  • when abdominal pain, nausea or vomiting are present unless directed by a doctor
  • if constipation lasts more than seven days
  • if you have difficulty swallowing

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

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

OTC - STOP USE SECTION

you experience rectal bleeding or fail to have a bowel movement, as these may be signs of a serious condition

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Mix this product with at least 8 ounces (a full glass) of water or other fluid. Taking this product without enough fluid may cause choking. See choking warning.

 adults and children 12 years and older one teaspoon 1 to 3 times daily
 children 6 to under 12 years of age 1/2 teaspoon 1 to 3 times daily
 children under 6 years of age consult a doctor

Other Information

SPL UNCLASSIFIED SECTION

  • each 12g dose contains Potassium 25mg, Sodium 5mg
  • laxatives, including bulk fibers, may affect how other medicines work, wait 1-2 hours before or after taking other medicines
  • tamper-evident bag sealed for your protection
  • do not use if seal of bag is broken or missing
  • do not discard Konsyl into any plumbing system
  • store below 86º F (30º C)
  • keep bag tightly closed to protect from excessive moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citric Acid, D&C Yellow No. 10, FD&C Yellow No. 6, Natural and Articial Orange Flavor, Sugar

Questions or Comments?

OTC - QUESTIONS SECTION

+1-410-822-5192 8:30 a.m. to 5 p.m. ET

Package Labeling: (0224-1915-89)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling: (0224-1915-85)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0224-19150224-1915-89, 0224-1915-85

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
D&C YELLOW NO. 1035SW5USQ3GIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
SUCROSEC151H8M554IACT
PSYLLIUM HUSK0SHO53407GACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d455d16a-4579-4db3-e053-2a95a90a0eeda0ad4bdd-0f2e-6630-e053-2a95a90a8ef62021-12-29WarningsExact identifier
spl id: d455d16a-4579-4db3-e053-2a95a90a0eed
spl set id: a0ad4bdd-0f2e-6630-e053-2a95a90a8ef6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.