Hemp with Flouride, Spearmint

Manufacturer
Lornamead
Effective date
2020-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:25:01

Label at a glance#

ProductHemp with Flouride, Spearmint
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure7 sections

Dosage and administration

adults and children 2 years of age and older: brush teeth thoroughly, preferably after each meal or at least twice per 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#

OTC - ACTIVE INGREDIENT SECTION

Sodium monofluorophosphate 0.76% (0.13% w/v fluoride ion) . . . Anticavity

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

aids in the prevention of dental cavities

WARNINGS SECTION

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 per 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 SAFETY INFORMATION

Tamper evident, use only if box seal is intact. Keep tube capped when not in use. When using this product, if irritation occurs, discontinue use. Keep out of reach of children.

INACTIVE INGREDIENT SECTION

glycerin, water, calcium carbonate, hydrated silica, xylitol, sodium bicarbonate, carrageenan, cannabis sativa (hemp) seed oil, sodium sauroyl sarcosinate, natural flavor, zinc citrate, benzyl alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sample ArtworkSample Artwork

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62721-003062721-0030-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
a87144c8-0cea-5abb-e053-2a95a90a9873a87144c8-0ce9-5abb-e053-2a95a90a98732020-06-19WarningsExact identifier
spl id: a87144c8-0cea-5abb-e053-2a95a90a9873
spl set id: a87144c8-0ce9-5abb-e053-2a95a90a9873

Reported adverse events (FAERS/openFDA)#

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