Grin

Manufacturer
GRIN NATURAL PRODUCTS LIMITED
Effective date
2020-06-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:30

Label at a glance#

ProductGrin
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure8 sections

Dosage and administration

For best results brush at least twice daily after meals and use in conjunction with Grin dental floss. Children 6 years and under should use a smear of toothpaste and have adult supervision until good habits are established. Do not swallow, spit out excess toothpaste.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Monofluorophosphate 0.76% (1000ppm)

Purpose

OTC - PURPOSE SECTION

Anticavity

Use

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Warnings

WARNINGS SECTION

If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center immediately. Do not use if you have an allergy to bees or bee products.

Directions

DOSAGE & ADMINISTRATION SECTION

For best results brush at least twice daily after meals and use in conjunction with Grin dental floss. Children 6 years and under should use a smear of toothpaste and have adult supervision until good habits are established. Do not swallow, spit out excess toothpaste.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Calcium Carbonate, Glycerine (Palm-free from Rapeseed), Aqua (Water), Xylitol, Lauryl Glucoside (Palm-free from Coconut), Sodium Bicarbonate, Chondrus crispus (Carrageenan) Gum, Foeniculum vulgare dulce (Fennel) Extract, Spearmint Flavour, Clove Flavour, Menthol, Xanthan Gum, Peppermint Oil, Organic NZ Sea Salt, Propolis cera (Propolis) Extract

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78420-002-012021-07-23C16284748780-1c7ccaba7-2307-fd44-e053-dadaa90aa01b4d9bf125-ea23-4f76-aa20-bf36185572da

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78420-002GRIN (SODIUM MONOFLUOROPHOSPHATE) PASTE [GRIN NATURAL PRODUCTS LIMITED]1Legacy NDC20200716_4d9bf125-ea23-4f76-aa20-bf36185572da.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78420-00278420-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

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
bd63a083-fc90-4bcf-8503-52cd125ce8ac4d9bf125-ea23-4f76-aa20-bf36185572da2020-06-30WarningsExact identifier
spl id: bd63a083-fc90-4bcf-8503-52cd125ce8ac
spl set id: 4d9bf125-ea23-4f76-aa20-bf36185572da

Reported adverse events (FAERS/openFDA)#

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