GOGLAMA NAF RNS MINT- sodium fluoirde rinse

GoGlama NaF RNS Mint by

Drug Labeling and Warnings

GoGlama NaF RNS Mint by is a Otc medication manufactured, distributed, or labeled by Ross Healthcare Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Adults and children 6 years of age and older:

use once a day after brushing your teeth with a toothpaste
remove cap
hold bottle upright and squeeze. Fill to FILL LINE
pour out. Only the correct 10 milliliters dose will pour out
vigorously swish 10 milliliters of rinse between your teeth for 1 minute and then spit out
do not swallow the rinse
do not eat or drink for 30 minutes after rinsing
instruct children under 12 years of age in good rinsing habits (to minimize swallowing)
supervise children as necessary until capable of using without supervision

children under 6 years of age: consult a dentist or doctor.

WARNINGS

Keep out of reach of children.

If more than used for rinsing is accidently swallowed, get medical help or contact Poison Control Center right away.

INACTIVE INGREDIENT

potassium sorbate, xylitol, sucralose, water

INDICATIONS & USAGE

Aids in the prevention of dental cavities

ACTIVE INGREDIENT

Sodium Fluoride 0.05%

KEEP OUT OF REACH OF CHILDREN

PURPOSE

Anticavity

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOGLAMA NAF RNS MINT 
sodium fluoirde rinse

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62007-700
Route of Administration	TOPICAL, DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)	0.04 mg  in 1 mL
XYLITOL (UNII: VCQ006KQ1E)	0.5 mg  in 1 mL
SUCRALOSE (UNII: 96K6UQ3ZD4)	0.01 mg  in 1 mL

Product Characteristics
Color		Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62007-700-16	1 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/22/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	11/22/2017

Labeler - Ross Healthcare Inc. (244249012)