NDC 82368-001 My Earthday Alpha Care Plus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82368 - J&p International Co., Ltd
- 82368-001 - My Earthday Alpha Care Plus
Product Packages
NDC Code 82368-001-02
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE (82368-001-01)
Product Details
What is NDC 82368-001?
What are the uses for My Earthday Alpha Care Plus?
Which are My Earthday Alpha Care Plus UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are My Earthday Alpha Care Plus 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:
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- CALCIUM GLYCEROPHOSPHATE (UNII: XWV9Z12C1C)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SAGE (UNII: 065C5D077J)
- CHAMOMILE (UNII: FGL3685T2X)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- XYLITOL (UNII: VCQ006KQ1E)
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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".