TIDALOVE- cool mint toothpaste tablets tablet, chewable

Tidalove by

Drug Labeling and Warnings

Tidalove by is a Otc medication manufactured, distributed, or labeled by Paranmare LLC, Productos de Bio Oxidacion Energetica SAPI de CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Sodium Fluoride 0.62mg (28 mg flouride ion)

Purpose

Anti-cavity

Use

Helps protect against cavities
Aids in the remineralization of enamel
Helps prevent tooth decay

Warnings

Do not swallow the toothpaste tablet.
Stop use and consult a dentist if irritation or sensitivity occurs.
Keep out of reach of children under 6 years old.
If more than the amount used for brushin is accidentall swallowed get advice from a doctor or contact a Poison Control Center.

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Adults and children 2 yrs & older: Chew 1 tablet until it breaks down, then brush teeth thoroughly at least twice a day or as directed by a dentist or physician.
  Children 2-6 yrs: Use 1 tablet under adult supervision to reduce the risk of swallowing.
  Children under 2 yrs: Ask a dentist or

Other information

Store in a cool, dry place.
Protect from excessive heat or moisture.
See expiration date on inner

Inactive ingredients

Xylitol, Microcrystalline Cellulose, Sodium Cocoyl Isethionate, Calcium Carbonate, Stevia Rebaudiana Extract, Acacia Senegal Gum, Hydroxyapatite, Mentha Piperita (Peppermint) Oil, Menthol, Sodium Bicarbonate, Silica, Zinc Citrate, Vitis Vinifera (Grape) Seed Extract, Pyrus Malus (Apple) Fruit Extract, Mentha Viridis (Spearmint) Leaf Oil, Tocopherol, Pyridoxine HCI, Ascorbic Acid, Rosmarinus Officinalis (Rosemary) Leaf Oil, Eucalyptus Globulus Leaf Oil, Limonene, Bamboo

QUESTIONS

www.tidalove.com

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

TIDALOVE 
cool mint toothpaste tablets tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82756-222
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.32 mg

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
EUCALYPTUS OIL (UNII: 2R04ONI662)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ACACIA (UNII: 5C5403N26O)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
TOCOPHEROL (UNII: R0ZB2556P8)
PYRIDOXINE HCL (UNII: 68Y4CF58BV)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
STEVIOSIDE (UNII: 0YON5MXJ9P)
MENTHOL (UNII: L7T10EIP3A)
ZINC CITRATE (UNII: K72I3DEX9B)
PEPPERMINT OIL (UNII: AV092KU4JH)
CALCIUM CARBONATE (UNII: H0G9379FGK)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYDROXYAPATITE (UNII: 91D9GV0Z28)
APPLE (UNII: B423VGH5S9)
ROSEMARY OIL (UNII: 8LGU7VM393)
VITIS VINIFERA SEED (UNII: C34U15ICXA)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	10mm
Flavor	PEPPERMINT	Imprint Code	NONE
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82756-222-62	62 in 1 POUCH; Type 0: Not a Combination Product	10/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	10/01/2025

Labeler - Paranmare LLC (049281321)

Establishment
Name	Address	ID/FEI	Business Operations
Productos de Bio Oxidacion Energetica SAPI de CV		951743619	manufacture(82756-222)