Metamucil

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-02
Label type
HUMAN OTC DRUG LABEL
Version
22
Source
daily-update
Hydrated at
2026-10-06 02:04:16

Label at a glance#

ProductMetamucil Therapy for Regularity
Active ingredientPSYLLIUM HUSK
Label structure18 sections

Indications and uses

for relief of occasional constipation (irregularity). This product generally produces bowel movement in 12 to 72 hours.

Dosage and administration

Put one dose into an empty glass.Mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid. Stir briskly and drink promptly. If mixture thickens, add more liquid and stir. For a lighter flavor experience and thinner drink, use more water. Adults 12 yrs. & older 1 packet in 8 oz of liquid at the first sign of irregularity. Can be taken up to 3 times daily. 6 – 11 yrs. 1/2 ...

Storage and handling

• each packet contains: potassium 30 mg; sodium 7 mg • Store below 86° F (30° C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each PACKET (12 g))

OTC - ACTIVE INGREDIENT SECTION

Psyllium husk approximately 3.4 g

Purpose

OTC - PURPOSE SECTION

Fiber laxative

Uses

INDICATIONS & USAGE SECTION

  • for relief of occasional constipation (irregularity). This product generally produces bowel movement in 12 to 72 hours.

Warnings

WARNINGS SECTION

Choking:

SPL UNCLASSIFIED SECTION

Taking this product without adequate fluid may cause it to swell and block your throat or esophagus andmay 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.

ALLERGY ALERT:

SPL UNCLASSIFIED SECTION

This product may cause allergic reactions in people sensitive to inhaled or ingested psyllium.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • abdominal pain, nausea or vomiting
  • a sudden change in bowel habits persisting for 2 weeks

Ask a doctor or pharmacist before use if you

OTC - ASK DOCTOR/PHARMACIST SECTION

are taking any other drug. Take this product 2 or more hours before or after other drugs. Laxatives may affect how other drugs work.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• constipation lasts more than 7 days
• rectal bleeding occurs
• you fail to have a bowel movement
These may be signs of a serious condition.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, contact a doctor or a PoisonControl Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Put one dose into an empty glass.Mix this product (child or adult dose) with at least 8 ounces (a full glass) of water or other fluid. Stir briskly and drink promptly. If mixture thickens, add more liquid and stir. For a lighter flavor experience and thinner drink, use more water.

Adults 12 yrs. & older1 packet in 8 oz of liquid at the first sign of irregularity.
Can be taken up to 3 times daily.
6 – 11 yrs.1/2 packet in 8 oz of liquid, up to 3 times daily
Under 6 yrs.Consult a doctor

As your body adjusts to increased fiber intake, you may experience changes in bowel habits or minor bloating.
New Users:Start with 1 dose per day; gradually increase to 3 doses per day as necessary.

Other information

STORAGE AND HANDLING SECTION

• each packet contains: potassium 30 mg; sodium 7 mg
• Store below 86° F (30° C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, FD&C Yellow No. 6, natural and artificial orange flavor, sucrose

Questions?

OTC - QUESTIONS SECTION

1-800-983-4237

SPL UNCLASSIFIED SECTION

INDIVIDUAL PACKETS SEALED FOR YOUR PROTECTION

SPL UNCLASSIFIED SECTION

DIST. BY PROCTER & GAMBLE

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MetaMUCIL ®

PSYLLIUM FIBER SUPPLEMENT THERAPY FOR REGULARITY

on-the-go!

30 packets

4-in-1 FIBER

HELPS SUPPORT:

Appetite Control*
Heart Health by Lowering Cholesterol†
Healthy Blood Sugar Levels*
Digestive Health*

made with REAL SUGAR

ORANGE

naturally and artificially flavored

†See back for information about soluble fiber and heart disease

30 - 0.43 OZ (12.2 g) POWDER PACKETS/NET WT 12.9 OZ (366 g)

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

023023

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix21178144023.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37000-023-04EA - Each37000-0230c0d4a36-8ef2-48d3-8a98-e1fb8900e1bd12015-10-02
37000-023-05GM - Gram37000-02335c83089-8f1e-4590-93e3-6fdabf9fef5012015-10-02
37000-023-10EA - Each37000-02391769a99-ef86-4e49-9701-f4cdb68f87e012020-06-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Psyllium HuskACTIVE INGREDIENT0SHO53407G2
Psyllium HuskACTIVE MOIETY0SHO53407G2
citric acid monohydrateINACTIVE INGREDIENT2968PHW8QP2
FD&C Yellow No. 6INACTIVE INGREDIENTH77VEI93A82
sucroseINACTIVE INGREDIENTC151H8M5542

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37000-02337000-023-04, 37000-023-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
212025-12-02full-release2026-06-01 01:19:12

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
sucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
FD&C Yellow No. 6FD&C YELLOW NO. 6H77VEI93A8POWDER / ORAL20 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
FD&C Yellow No. 6FD&C YELLOW NO. 6H77VEI93A8POWDER / ORAL20 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
sucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
sucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
citric acid monohydrateCITRIC ACID MONOHYDRATE2968PHW8QPPOWDER / ORAL840 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
citric acid monohydrateCITRIC ACID MONOHYDRATE2968PHW8QPPOWDER / ORAL840 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
citric acid monohydrateCITRIC ACID MONOHYDRATE2968PHW8QPPOWDER / ORAL840 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
FD&C Yellow No. 6FD&C YELLOW NO. 6H77VEI93A8POWDER / ORAL20 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

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
Metamucil Therapy for RegularityPSYLLIUM HUSKThe Procter & Gamble Manufacturing Company12d030b0-df97-4dd6-88ba-e9fe863c95ea2025-12-02WarningsExact identifier
ndc (package): 37000-023-04
ndc (package): 37000-023-10
ndc (product): 37000-023
ndc11 (package): 37000002304
ndc11 (package): 37000002310
spl set id: 12d030b0-df97-4dd6-88ba-e9fe863c95ea

Reported adverse events (FAERS/openFDA)#

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