FDA.reportPublic FDA data

Charm Tex FLUORIDE

Product NDC
71035-001
11-digit product format
710350001
Labeler code
71035
Product ID
71035-001_3ca5d2b2-d884-a6b1-e063-6394a90a970d
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM MONOFLUOROPHOSPHATE
Dosage form
PASTE, DENTIFRICE
Route
TOPICAL
Labeler
Yangzhou Hongshengding Chemical Co.,Ltd.
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-13
Substance
SODIUM MONOFLUOROPHOSPHATE
Active strength
.1 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Charm Tex FLUORIDE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM MONOFLUOROPHOSPHATE.1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
C810JCZ56QInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
545626Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
63a69664-8611-4d69-b871-8d1d5b553e5cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71035-001-01Charm Tex FLUORIDE720 in 1 PACKAGEPASTE, DENTIFRICE7202
71035-001-01Charm Tex FLUORIDE17 g in 1 TUBEPASTE, DENTIFRICE172
71035-001-02Charm Tex FLUORIDE24 g in 1 TUBEPASTE, DENTIFRICE242
71035-001-02Charm Tex FLUORIDE720 in 1 PACKAGEPASTE, DENTIFRICE7202
71035-001-03Charm Tex FLUORIDE43 g in 1 TUBEPASTE, DENTIFRICE432
71035-001-03Charm Tex FLUORIDE144 in 1 PACKAGEPASTE, DENTIFRICE1442
71035-001-04Charm Tex FLUORIDE78 g in 1 TUBEPASTE, DENTIFRICE782
71035-001-04Charm Tex FLUORIDE144 in 1 PACKAGEPASTE, DENTIFRICE1442
71035-001-05Charm Tex FLUORIDE130 g in 1 TUBEPASTE, DENTIFRICE1302
71035-001-05Charm Tex FLUORIDE60 in 1 PACKAGEPASTE, DENTIFRICE602
71035-001-06Charm Tex FLUORIDE181 g in 1 TUBEPASTE, DENTIFRICE1812
71035-001-06Charm Tex FLUORIDE60 in 1 PACKAGEPASTE, DENTIFRICE602

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 34 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Listerine Gum Therapy Glacier MintEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLKenvue Brands LLCed6889b6-58db-41cf-e053-2a95a90a7de22024-11-11WarningsExact identifier
application number: M022
Listerine FreshBurst AntisepticEUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOLKenvue Brands LLC62b5c3ee-01cc-4c4e-9f28-e7dafa7372d82024-11-11WarningsExact identifier
application number: M022
Listerine Ultraclean Antiseptic Cool MintEUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOLKenvue Brands LLCdd3729c2-fd05-4db0-a542-487bb0f9001f2024-11-11WarningsExact identifier
application number: M022
Listerine Cool Mint AntisepticEUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOLKenvue Brands LLC9e97e4f8-80c2-44e0-862c-0dfca392a4362024-11-11WarningsExact identifier
application number: M022
Orajel 2X Medicated GelORAL PAIN RELIEVERChurch & Dwight Co., Inc.262be295-4eaf-3136-e063-6294a90a7dcc2024-11-05WarningsExact identifier
application number: M022
BIOTENE Fresh Mint OriginalSODIUM FLUORIDEHaleon US Holdings LLC1101c17f-c848-4cd5-a7cd-679b59dbe1bf2024-11-05WarningsExact identifier
application number: M022
bioteneSODIUM MONOFLUOROPHOSPHATEHaleon US Holdings LLCa47a6502-efb2-4072-9562-cbe293531c2b2024-11-04WarningsExact identifier
application number: M022
Amosan Oral Wound Cleanser CherrySODIUM PERBORATE MONOHYDRATEVintage Brands Limiteda0e145c8-6b08-40be-ae4f-5678c4a78b1e2024-10-30WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLC043bfbc3-c33b-78b7-e063-6294a90a1a5a2024-10-29WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLC043bfbc3-c33a-78b7-e063-6294a90a1a5a2024-10-29WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLC043a3cb4-f560-0ffd-e063-6394a90a2ff62024-10-29WarningsExact identifier
application number: M022
Amosan Oral Wound Cleanser MintSODIUM PERBORATE MONOHYDRATEVintage Brands Limitedbe57ca56-834f-4170-a407-f193484d8b0a2024-10-29WarningsExact identifier
application number: M022
SENSODYNE PRONAMEL Intensive Enamel Repair Clean MintSODIUM FLUORIDEHaleon US Holdings LLC817c0dad-d109-428e-adb5-3354604acc942024-10-28WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLC1f3d68f6-afd6-42e7-b3e5-210228c8e7de2024-10-28WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals LLC0dd15227-6603-42ac-9a5f-f2dc49e0382a2024-10-28Warnings, Adverse reactionsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLC0605d5d6-82bd-415e-b5cb-e273f934a4a72024-10-28WarningsExact identifier
application number: M022
HurriCaine Topical Anesthetic LiquidBENZOCAINEBeutlich Pharmaceuticals, LLCf70fa3fc-cd65-4a80-9efd-129e98fd39982024-10-28WarningsExact identifier
application number: M022
Sore Throat Relief MentholPHENOLChain Drug Consortiumaf661ef0-cdc3-4146-8ae5-59795aa496502024-10-28WarningsExact identifier
application number: M022
Sore Throat Relief Cherry FlavorPHENOLChain Drug Consortiuma9cf9829-4b70-44fa-9719-240b65c067242024-10-28WarningsExact identifier
application number: M022
Ear Wax Removal Aid DropsCARBAMIDE PEROXIDEPHARMACY VALUE ALLIANCE, LLC85ae80c1-2bc2-4c90-9559-63510d03e7392024-10-28WarningsExact identifier
application number: M022

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
545626sodium monofluorophosphate 0.76 % ToothpastePSN63a69664-8611-4d69-b871-8d1d5b553e5c2
545626sodium monofluorophosphate 0.0076 MG/MG ToothpasteSCD63a69664-8611-4d69-b871-8d1d5b553e5c2
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )ToothpasteSY63a69664-8611-4d69-b871-8d1d5b553e5c2
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )ToothpasteSY63a69664-8611-4d69-b871-8d1d5b553e5c2
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )ToothpasteSY63a69664-8611-4d69-b871-8d1d5b553e5c2
545626sodium monofluorophosphate 0.76 % (fluoride ion 0.15 % )ToothpasteSY63a69664-8611-4d69-b871-8d1d5b553e5c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71035-001-0171035000101720 TUBE in 1 PACKAGE (71035-001-01) / 17 g in 1 TUBE720 tube2025-06-13NoNoCurrent
71035-001-0271035000102720 TUBE in 1 PACKAGE (71035-001-02) / 24 g in 1 TUBE720 tube2025-06-13NoNoCurrent
71035-001-0371035000103144 TUBE in 1 PACKAGE (71035-001-03) / 43 g in 1 TUBE144 tube2025-06-13NoNoCurrent
71035-001-0471035000104144 TUBE in 1 PACKAGE (71035-001-04) / 78 g in 1 TUBE144 tube2025-06-13NoNoCurrent
71035-001-057103500010560 TUBE in 1 PACKAGE (71035-001-05) / 130 g in 1 TUBE60 tube2025-06-13NoNoCurrent
71035-001-067103500010660 TUBE in 1 PACKAGE (71035-001-06) / 181 g in 1 TUBE60 tube2025-06-13NoNoCurrent