CHARM TEX FLUORIDE- sodium monofluorophosphate paste, dentifrice

Charm Tex FLUORIDE by

Drug Labeling and Warnings

Charm Tex FLUORIDE by is a Otc medication manufactured, distributed, or labeled by Yangzhou Hongshengding Chemical Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

SODIUM MONOFLUOROPHOSPHATE: 0.76% (0.1% Fluoride ion)

PURPOSE

Purpose: Anticavity

Uses

Help protect against cavities.

Warnings

Keep out of the reach of children under 6 years of age. If more than used for brushing is accidently swallowed, get medical help or contact a Poison Control Center immediately.

Keep out of reach of children.

Directions

• Adults and children 6 years of age and older:Brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by a dentist or a physician.
• Children 2 to 6 years: Use only a pea sized amount and supervise children's brushing and rinsing to minimize swallowing
• Children under 2 years: Ask a dentist or physician

INACTIVE INGREDIENT

Sorbitol, Silica, Calcium Carbonate, Methylparaben Sodium, Propylparaben Sodium, Flavor, Sodium Saccharin, Water,  SCMC, Sodium Lauryl Sulfate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CHARM TEX FLUORIDE 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71035-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
CALCIUM CARBONATE (UNII: H0G9379FGK)
WATER (UNII: 059QF0KO0R)
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71035-001-01	720 in 1 PACKAGE	06/13/2025
1		17 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 71035-001-02	720 in 1 PACKAGE	06/13/2025
2		24 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 71035-001-03	144 in 1 PACKAGE	06/13/2025
3		43 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 71035-001-04	144 in 1 PACKAGE	06/13/2025
4		78 g in 1 TUBE; Type 0: Not a Combination Product
5	NDC: 71035-001-05	60 in 1 PACKAGE	06/13/2025
5		130 g in 1 TUBE; Type 0: Not a Combination Product
6	NDC: 71035-001-06	60 in 1 PACKAGE	06/13/2025
6		181 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	M022	06/13/2025

Labeler - Yangzhou Hongshengding Chemical Co.,Ltd. (543774755)

Registrant - Yangzhou Hongshengding Chemical Co.,Ltd. (543774755)

Establishment
Name	Address	ID/FEI	Business Operations
Yangzhou Hongshengding Chemical Co.,Ltd.		543774755	manufacture(71035-001)