NDC 71775-050 Dr. Gingiva
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 71775-050?
What are the uses for Dr. Gingiva?
Which are Dr. Gingiva UNII Codes?
The UNII codes for the active ingredients in this product are:
- STANNOUS FLUORIDE (UNII: 3FTR44B32Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Dr. Gingiva Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- ZANTHOXYLUM NITIDUM ROOT (UNII: L2CQZ81759)
- CLINOPODIUM CHINENSE WHOLE (UNII: 29350ODC51)
- SODIUM COPPER CHLOROPHYLLIN (UNII: 1D276TYV9O)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Dr. Gingiva?
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.16 % ) Toothpaste
- RxCUI: 416784 - stannous fluoride 0.00454 MG/MG Toothpaste
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.15 % ) Toothpaste
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".