NDC 71035-200

Charm Tex Fluoride

Sodium Fluoride

Charm Tex Fluoride is a Dental Paste in the Human Otc Drug category. It is labeled and distributed by Yangzhou Hongshengding Chemical Co.,ltd.. The primary component is Sodium Monofluorophosphate.

Product ID71035-200_62175f7d-6bea-2fb8-e053-2991aa0adb4b
NDC71035-200
Product TypeHuman Otc Drug
Proprietary NameCharm Tex Fluoride
Generic NameSodium Fluoride
Dosage FormPaste
Route of AdministrationDENTAL
Marketing Start Date2016-10-20
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart355
Labeler NameYangzhou Hongshengding Chemical Co.,Ltd.
Substance NameSODIUM MONOFLUOROPHOSPHATE
Active Ingredient Strength1 g/100g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71035-200-15

5 g in 1 TUBE (71035-200-15)
Marketing Start Date2016-10-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71035-200-14 [71035020014]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-07 [71035020007]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-04 [71035020004]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-09 [71035020009]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-08 [71035020008]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-15 [71035020015]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-12 [71035020012]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-02 [71035020002]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-03 [71035020003]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-05 [71035020005]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-10 [71035020010]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-06 [71035020006]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-11 [71035020011]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-16 [71035020016]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-01 [71035020001]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71035-200-13 [71035020013]

Charm Tex Fluoride PASTE
Marketing CategoryOTC monograph final
Application Numberpart355
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SODIUM MONOFLUOROPHOSPHATE.76 g/100g

OpenFDA Data

SPL SET ID:3f4d3a9f-b320-3f8e-e054-00144ff88e88
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 545626

    • NDC Crossover Matching brand name "Charm Tex Fluoride" or generic name "Sodium Fluoride"

    NDCBrand NameGeneric Name
    71035-200Charm Tex FluorideCharm Tex Fluoride
    51289-200Charm Tex FluorideCharm Tex Fluoride
    73343-003Charm Tex FluorideCharm Tex Fluoride
    0135-0234AQUAFRESHsodium fluoride
    0126-0021ColgateSODIUM FLUORIDE
    0126-0034Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Gushing Grape FluorideSODIUM FLUORIDE
    0126-0032Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Mint FluorideSODIUM FLUORIDE
    0041-1421Oral-BSodium Fluoride
    0126-0131Phos-FlurSodium Fluoride
    0126-0135Phos-Flur Ortho DefenseSODIUM FLUORIDE
    0126-0138Phos-Flur Ortho DefenseSODIUM FLUORIDE
    0126-0139Phos-Flur Ortho DefenseSODIUM FLUORIDE
    0126-0074PrevidDent 5000 Booster Plus SpearmintSodium Fluoride
    0126-0016PreviDentSodium fluoride
    0126-0075PreviDentSodium fluoride
    0126-0076PreviDentSodium fluoride
    0126-0179PreviDentSodium Fluoride
    0126-0286PreviDentSodium Fluoride
    0126-0287PreviDentSodium Fluoride
    0126-0072PreviDent 5000 Booster Plus FruitasticSodium Fluoride
    0126-0033PreviDent Alcohol FreeSodium Fluoride
    0126-0088PreviDent Fresh MintSodium Fluoride
    0126-0289PreviDent OrthoDefenseSODIUM FLUORIDE
    0126-0288PreviDent Very BerrySodium Fluoride
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