FDA.reportPublic FDA data

Killfire Mouthwash

Manufacturer
Pharmacal-International. Co., Ltd. | Ecoworld Co .,ltd
Effective date
2024-10-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:29:16

Label at a glance#

ProductKillfire Mouthwash
Active ingredientSODIUM FLUORIDE
Label structure2 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride (0.02%)

Purpose

OTC - PURPOSE SECTION

  • Anticavity mouthwash

Use

INDICATIONS & USAGE SECTION

  • Aids in prevention of dental cavities

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rinse mouth with this Killfire Mouthwash about 10~15ml for 30 seconds then expel

Average daily dose

  •  Use twice a day after brushing, meals, and before social occasions.

Warnings

WARNINGS SECTION

  • Keep out of reach of children.
  • Children under 7 years or younger must have parent supervision.
  • Do not swallow. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Fluoride, Allantoin, Glycerin, Xylitol, Acetic acid, Sodium acetate, Malic acid, Sodium Benzoate, GreenTea Extract, Sodium Saccharin, flavoring, Polyoxyethylenehardened castor oil, L-Menthol, Cacao Color, Purified water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313029sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral RinsePSN6
313029sodium fluoride 0.2 MG/ML MouthwashSCD6
313029sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral RinseSY6
313029sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral RinseSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24765-132-012025-07-29C16284748780-1f386c649-b691-0266-e053-dadaa90a7c1a11deebbb-4ad2-4c8b-b1d4-51223284a118
24765-132-012023-02-02C16284748780-1f386c649-b691-0266-e053-dadaa90a7c1a11deebbb-4ad2-4c8b-b1d4-51223284a118
24765-132-012023-01-30C16284748780-1f386c649-b691-0266-e053-dadaa90a7c1a11deebbb-4ad2-4c8b-b1d4-51223284a118

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24765-132-01Killfire Mouthwash500 mL in 1 BOTTLE, PLASTICRINSE5006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24765-132KILLFIRE MOUTHWASH (SODIUM FLUORIDE) RINSE [PHARMACAL-INTERNATIONAL. CO., LTD.]6Legacy NDC, 1 package rows20241027_11deebbb-4ad2-4c8b-b1d4-51223284a118.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24765-13224765-132-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
GLYCERINPDC6A3C0OXIACT
XYLITOLVCQ006KQ1EIACT
ACETIC ACIDQ40Q9N063PIACT
SODIUM ACETATE4550K0SC9BIACT
MALIC ACID817L1N4CKPIACT
SODIUM BENZOATEOJ245FE5EUIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
SACCHARIN SODIUM ANHYDROUSI4807BK602IACT
POLYOXYL 35 CASTOR OIL6D4M1DAL6OIACT
RACEMENTHOLYS08XHA860IACT
PROPOLIS WAX6Y8XYV2NOFIACT
WATER059QF0KO0RIACT
SODIUM FLUORIDE8ZYQ1474W7ACTIM

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
254e6bec-594e-2ab9-e063-6394a90aacd011deebbb-4ad2-4c8b-b1d4-51223284a1182024-10-25WarningsExact identifier
spl id: 254e6bec-594e-2ab9-e063-6394a90aacd0
spl set id: 11deebbb-4ad2-4c8b-b1d4-51223284a118

Reported adverse events (FAERS/openFDA)#

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