Escopinio PHYTO alpha Toothpaste

Manufacturer
Zion Synthetic Fiber Corporation Limited
Effective date
2010-01-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:17

Label at a glance#

ProductEscopinio PHYTO alpha Toothpaste
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure5 sections

Storage and handling

Care and Handling: Keep the lid tightly closed after using. Keep at a room temperature

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Sodium Monofluorophosphate

INACTIVE INGREDIENT SECTION

Other Ingredients:
Water, Dicalcium Phosphodihydrate, Tocopheryl Acetate, Sodium Benzoate, d-Sorbitol, Sodium Carboxymethylcellulose, Silica, Monosodium Phosphate, Sodium Lauryl Sulfate, Monooleic Sorbate, Tetrasodium Pyrophosphate, Sodum Saccharin, Xylitol, Mentha (peppermint), Fragrance HF 30302, Sage Oil, Myrrh Extract, Cardamom Extract, Blue FCF #1, Yellow #4, Titanium Dioxide

OTC - WHEN USING SECTION

Directions:
Adults and children 2 years and older:
Brush teeth thoroughly preferably after each meal or at least twice a day or as directed by your dentist.

Children under 6 years of age:
To minimize swallowing, use a pea sized amount and supervise brushing until good habits are established.

Children under 2 years: Ask a dentist or physician

STORAGE AND HANDLING SECTION

Care and Handling:
Keep the lid tightly closed after using.
Keep at a room temperature

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BOX LABEL
BOX LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
545626sodium monofluorophosphate 0.76 % ToothpastePSN1
545626sodium monofluorophosphate 0.0076 MG/MG ToothpasteSCD1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )ToothpasteSY1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )ToothpasteSY1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )ToothpasteSY1
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.15 % )ToothpasteSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44781-447-812019-10-21C16284748780-1956f9ecf-d8de-621f-e053-dbdaa90a74ad491a242f-7c80-464d-82f6-52ecf8d56e82

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44781-447-81Escopinio PHYTO alpha Toothpaste120 g in 1 TUBEPASTE1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44781-447ESCOPINIO PHYTO ALPHA TOOTHPASTE (SODIUM MONOFLUOROPHOSPHATE) PASTE [ZION SYNTHETIC FIBER CORPORATION LIMITED]1Legacy NDC, 1 package rows20100122_491a242f-7c80-464d-82f6-52ecf8d56e82.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM MONOFLUOROPHOSPHATEACTIVE INGREDIENTC810JCZ56Q1
FLUORIDE IONACTIVE MOIETYQ80VPU408O1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44781-44744781-447-81

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM MONOFLUOROPHOSPHATEC810JCZ56QACTIB

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
2e7c2d4f-ea08-4398-affe-2548560fa48d491a242f-7c80-464d-82f6-52ecf8d56e822010-01-21Exact identifier
spl id: 2e7c2d4f-ea08-4398-affe-2548560fa48d
spl set id: 491a242f-7c80-464d-82f6-52ecf8d56e82

Reported adverse events (FAERS/openFDA)#

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