Greenco

Manufacturer: Greenco Industries, Inc.
Effective date: 2017-12-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:53:19

Label at a glance#

ProductGreenco

Active ingredientSODIUM FLUORIDE

Label structure8 sections

Indications and uses

Aids in the prevention of dental cavities.

Dosage and administration

Adults and children 2 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 2 years of age: consult a dentist or doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.24%

Purpose

OTC - PURPOSE SECTION

Anticavity

Uses

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. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 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 2 years of age: consult a dentist or doctor.

Other informaiton

OTHER SAFETY INFORMATION

For your protection, this tube has a foil seal under the cap.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sorbitol, Hydrated Silica, Water, Glycerin, PEG 12, Sodium Lauryl Sulfate, Cellulose Gum, Flavor, Sodium Benzoate, Disodium Phosphate, Sodium Saccharin, FD&C Blue #1

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fresh Mint Tartar Control

Greenco

NET WT. 1.5oz. (43grams) Fluoride Toothpaste

Greenco_mint_paste

Greenco_mint_toothpaste

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
416783	sodium fluoride 0.24 % Toothpaste	PSN	2
416783	sodium fluoride 0.0024 MG/MG Toothpaste	SCD	2
416783	sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste	SY	2
416783	sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste	SY	2
416783	sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63372-0596-1	2020-01-31	C162847	48780-1	9d75b9d0-f379-f424-e053-dadaa90a57ce	Greenco - Toothpaste
63372-0596-2	2020-01-31	C162847	48780-1	9d75b9d0-f379-f424-e053-dadaa90a57ce	Greenco - Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63372-0596-1	Greenco	43 g in 1 TUBE	PASTE, DENTIFRICE	43		2
63372-0596-2	Greenco	85 g in 1 TUBE	PASTE, DENTIFRICE	85		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63372-0596	GREENCO PASTE, DENTIFRICE [GREENCO INDUSTRIES, INC.]	2	Legacy NDC, 2 package rows	20171207_085ea133-ad0a-1cce-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

Greenco
SACCHARIN SODIUM
SODIUM BENTONITE
GLYCERIN
POLYETHYLENE GLYCOL 600
CARBOXYMETHYLCELLULOSE
SODIUM LAURYL SULFATE
SILICON DIOXIDE
SODIUM FLUORIDE
FLUORIDE ION
WATER
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
SORBITOL
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63372-0596	63372-0596-2, 63372-0596-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SACCHARIN SODIUM	SB8ZUX40TY	IACT
SODIUM BENTONITE	K1BPI94O04	IACT
GLYCERIN	PDC6A3C0OX	IACT
POLYETHYLENE GLYCOL 600	NL4J9F21N9	IACT
CARBOXYMETHYLCELLULOSE	05JZI7B19X	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIM
WATER	059QF0KO0R	IACT
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS	22ADO53M6F	IACT
SORBITOL	506T60A25R	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
429f845a-0ab2-735f-e054-00144ff8d46c			085ea133-ad0a-1cce-e054-00144ff8d46c	2017-12-06	Warnings	Exact identifier spl id: 429f845a-0ab2-735f-e054-00144ff8d46c spl set id: 085ea133-ad0a-1cce-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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