BYUN RAK

Manufacturer
OASIS TRADING
Effective date
2019-03-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:58:55

Label at a glance#

ProductBYUN RAK
Active ingredientSENNA LEAF, ALOE, MAGNOLIA OFFICINALIS BARK, PAEONIA LACTIFLORA ROOT, RHUBARB, PLANTAGO INDICA SEED COAT
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

rhubarb ....................... 200mg
Alexandrian Senna ............................. 500mg
Peony root ......................... 200mg
Plantago spp. .........................2000mg
Officinal Magnolia .......... 200mg
Aloe ......................... 200mg

OTC - PURPOSE SECTION

■relieves occasional constipation(Irregularity)
■generally produces bowel movement in 6 to 12 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

■ adult and children 15 years of age and older: 1envelop twice daily
■ children 11 to under 15 years of age: 2/3 envelop twice daily
■ children 7 to under 11 years of age: 1/2 envelop twice daily
■ children 3 to under 7 years of age: 1/3 envelop twice daily
■ children under 3 years of age: ask a doctor

WARNINGS SECTION

Do not use laxative products when abdominal pain, nausea or vomiting are present unless directed by a doctor
Ask a doctor before use if you have noticed a sudden change in bowel habits that persists over a period of 2 weeks
Ask a doctor before use if you have noticed a sudden change in bowel habits that persists over a period of 2 weeks
When using this product
Do not use for a period longer than 1 weeks
Stop use and ask a doctor if rectal bleeding or failure to have a bowel movement occur after use of a laxative. These may be signs of a serious condition
If pregnant 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 contral center right away.

INACTIVE INGREDIENT SECTION

corn starch, Sodium Carboxymethyl Cellulose

DOSAGE & ADMINISTRATION SECTION

For oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
RHUBARB Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72689-0043-12021-01-29C16284748780-1ba0f9c33-2578-a910-e053-dadaa90a0b8584a633dc-bd63-0571-e053-2a91aa0a6df8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72689-0043-1BYUN RAK20 in 1 BOXGRANULE201
72689-0043-1BYUN RAK4 g in 1 POUCHGRANULE41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72689-0043BYUN RAK (RHUBARB, ALEXANDRIAN SENNA, PEONY ROOT, PLANTAGO SPP., OFFICINAL MAGNOLIA, MAGNOLIAE CORTEX, ALOE) GRANULE [OASIS TRADING]1Legacy NDC, 2 package rows20190322_84a633dc-bd63-0571-e053-2a91aa0a6df8.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72689-004372689-0043-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
84a6a29c-1379-f375-e053-2991aa0a1c1484a633dc-bd63-0571-e053-2a91aa0a6df82019-03-21WarningsExact identifier
spl id: 84a6a29c-1379-f375-e053-2991aa0a1c14
spl set id: 84a633dc-bd63-0571-e053-2a91aa0a6df8

Reported adverse events (FAERS/openFDA)#

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