POP HINT OF MINT- sodium fluoride paste, dentifrice 
LG H&H CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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POP Hint Of Mint Toothpaste 120g

Drug Facts

Drug Facts

Active Ingredient

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

Purpose

Anticavity toopaste

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

Inactive Ingredients

WATER, SORBITOL, HYDRATED SILICA, SODIUM LAURYL SULFATE, GLYCERIN, CELLULOSE GUM, FLAVOR, TETRASODIUM PYROPHOSPHATE, ZINC STEARATE, XANTHAN GUM, TITANIUM DIOXIDE, SORBITAN OLEATE, SODIUM SACCHARIN, HYDROXYAPATITE, NIACINAMIDE, TOCOPHERYL ACETATE, XYLITOL

Questions?

1-866-993-4709

Principal Display Panel - 120 g Tube Carton

POP

Playful. Original. Personal

REPAIRS ENAMEL
PREVENTS CAVITIES
FRESHENS BREATH


HINT OF MINT

Fluoride Toothpaste
with Hydroxyapatite &
Vitamins E and B3

NET WT. 4.2 OZ. (120 G)

DIST. LG H&H CO., LTD.
58, SAEMUNAN-RO, JONGNO-GU, SEOUL, KOREA
www.oralcarebypop.com

MADE IN KOREA

POP_Hint_of_Mint_120g_IC

POP_Hint_of_Mint_120g_OC

POP HINT OF MINT 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-571
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.4 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL (UNII: 506T60A25R)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
NIACINAMIDE (UNII: 25X51I8RD4)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
WATER (UNII: 059QF0KO0R)  
ZINC STEARATE (UNII: H92E6QA4FV)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
XYLITOL (UNII: VCQ006KQ1E)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53208-571-201 in 1 CARTON09/18/2023
1120 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35509/18/2023
Labeler - LG H&H CO., LTD. (688276187)
Establishment
NameAddressID/FEIBusiness Operations
Tai Guk Pharma. Co., Ltd.689060246manufacture(53208-571)

Revised: 9/2023
Document Id: 05b2273a-59f8-1a25-e063-6394a90a888f
Set id: 05b25083-12f3-7a85-e063-6394a90a492e
Version: 1
Effective Time: 20230918
 
LG H&H CO., LTD.