NDC 53208-449 Perioe Lucky Fresh - Breath Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-449 - Perioe Lucky Fresh - Breath Care
Product Packages
NDC Code 53208-449-02
Package Description: 1 TUBE in 1 CARTON / 130 g in 1 TUBE (53208-449-01)
Product Details
What is NDC 53208-449?
What are the uses for Perioe Lucky Fresh - Breath Care?
Which are Perioe Lucky Fresh - Breath Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM GLYCEROPHOSPHATE (UNII: XWV9Z12C1C)
- CALCIUM GLYCEROPHOSPHATE (UNII: XWV9Z12C1C) (Active Moiety)
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Perioe Lucky Fresh - Breath Care 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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SORBITOL (UNII: 506T60A25R)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Perioe Lucky Fresh - Breath Care?
- RxCUI: 1046415 - sodium monofluorophosphate 0.76 % / calcium glycerophosphate 0.13 % Toothpaste
- RxCUI: 1046415 - calcium glycerophosphate 1.3 MG/ML / sodium monofluorophosphate 7.6 MG/ML Toothpaste
- RxCUI: 1046415 - calcium glycerophosphate 0.13 % / sodium monofluorophosphate 0.76 % 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".