PERIOE POP COMPLETE PROTECTION PREBIOTIC MINT BLAST- sodium fluoride paste, dentifrice

PERIOE POP Complete Protection Prebiotic by

Drug Labeling and Warnings

PERIOE POP Complete Protection Prebiotic by is a Otc medication manufactured, distributed, or labeled by Tai Guk Pharm. Co., Ltd., LG H&H Co., Ltd., Tai Guk Pharma. Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active Ingredient

SODIUM FLUORIDE 0.243% (0.14% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

• helps protect against cavities

WARNINGS

Warnings

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children under 6 years of age.
Do not swallow. If you accidentally swallow more than used for brushing, seek professional assistance or contact a Poison Control Center right away. If an allergic reaction develops, discontinue use immediately.

Directions

• 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.
• do not swallow
• to minimize swallowing use a pea-sized amount in children under 6
• supervise children's brushing until good habits are established.
• children under 2 years: ask a dentist.

Inactive Ingredients

WATER, SORBITOL, HYDRATED SILICA, SODIUM LAURYL SULFATE, GLYCERIN, FLAVOR, CELLULOSE GUM, TETRASODIUM PYROPHOSPHATE, XANTHAN GUM, TITANIUM DIOXIDE, SORBITAN OLEATE, SODIUM SACCHARIN, CHARCOAL POWDER, BIFIDA FERMENT EXTRACT FILTRATE, SODIUM CHLORIDE, TOCOPHERYL ACETATE, XYLITOL

Questions?

1-800-367-2866

Distributed by

DISTR. LG H&H CO., LTD.
58, SAEMUNAN-RO, JONGNO-GU, SEOUL, KOREA
www.lghnh.com
LG H&H
MADE IN KOREA

Principal Display Panel - 120 g Tube Carton

PERIOE

POP

COMPLETE
PROTECTION

PREBIOTIC
TOOTHPASTE

MINT BLAST
WITH FLUORIDE

120g net wt. 4.2 oz.

INGREDIENTS AND APPEARANCE

PERIOE POP COMPLETE PROTECTION PREBIOTIC  MINT BLAST
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43136-603
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.4 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MICA (UNII: V8A1AW0880)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
XYLITOL (UNII: VCQ006KQ1E)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
XANTHAN GUM (UNII: TTV12P4NEE)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MINT (Blast)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43136-603-01	1 in 1 CARTON	02/17/2023
1		120 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	02/17/2023

Labeler - Tai Guk Pharm. Co., Ltd. (689060246)

Registrant - LG H&H Co., Ltd. (688276187)

Establishment
Name	Address	ID/FEI	Business Operations
Tai Guk Pharma. Co., Ltd.		689060246	manufacture(43136-603)