Bamboo Salt 160g

Manufacturer
Hanul Trading Co., Ltd. | KOCO TRADING CO., INC. | LG Household&Health Care
Effective date
2017-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:51:43

Label at a glance#

ProductBamboo Salt 160g
Active ingredientSODIUM LAURYL SULFATE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium Lauryl Sulfate 0.76%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Sorbitol Solution, Water(Aqua), Hydrated Silica, Flavor(Aroma), PEG-6, Xanthan Gum, Cellulose Gum, Poloxamer 407, Sodium Saccharin, Methyl Paraben, Sodium Chloride, Tocopheryl Acetate, Sodium Bisulfite, Camelia Sinensis Leaf Extract, D&C Yellow NO.10(CI47005), FD&C Blue No.1 (CI 42090)

PURPOSE

OTC - PURPOSE SECTION

Purpose: Oral Health Care

WARNINGS

WARNINGS SECTION

Warnings: Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age.

Direction

INDICATIONS & USAGE SECTION

Direction: Adults and children 6 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day, or as directed by a dentist or doctor, Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 6 years of age: Consult a dentist or doctor

Direction

DOSAGE & ADMINISTRATION SECTION

Direction: Adults and children 6 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day, or as directed by a dentist or doctor, Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 6 years of age: Consult a dentist or doctor

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69642-1400-22020-01-31C16284748780-19d75b9d0-07c0-f424-e053-dadaa90a57ce9d346fda-1da6-4540-93b0-ab9d06e28280

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69642-1400-1Bamboo Salt 160g160 g in 1 TUBEPASTE, DENTIFRICE1602
69642-1400-2Bamboo Salt 160g1 in 1 CARTONPASTE, DENTIFRICE12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69642-1400BAMBOO SALT 160G (SODIUM LAURYL SULFATE) PASTE, DENTIFRICE [HANUL TRADING CO., LTD.]2Legacy NDC, 2 package rows20170625_9d346fda-1da6-4540-93b0-ab9d06e28280.zip

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
69642-140069642-1400-1, 69642-1400-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM LAURYL SULFATE368GB5141JACTIB

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
52c1413e-2814-367b-e054-00144ff88e889d346fda-1da6-4540-93b0-ab9d06e282802017-06-24WarningsExact identifier
spl id: 52c1413e-2814-367b-e054-00144ff88e88
spl set id: 9d346fda-1da6-4540-93b0-ab9d06e28280

Reported adverse events (FAERS/openFDA)#

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