NDC 71727-102 Marine Purifying
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71727 - Imode Korea, Inc.
- 71727-102 - Marine Purifying
Product Packages
NDC Code 71727-102-03
Package Description: 5 POUCH in 1 BOX / 1 PATCH in 1 POUCH (71727-102-02) / 27 mL in 1 PATCH (71727-102-01)
Product Details
What is NDC 71727-102?
What are the uses for Marine Purifying?
Which are Marine Purifying UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Marine Purifying 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CASTANEA CRENATA SHELL (UNII: MTF3V701OO)
- MALVA SYLVESTRIS FLOWERING TOP (UNII: X1U1U0N90J)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- PRIMULA VERIS (UNII: W6LFQ57E4M)
- ALCHEMILLA XANTHOCHLORA FLOWERING TOP (UNII: 9M289NKI69)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- MORINGA OLEIFERA SEED (UNII: TIX5482832)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- ALCOHOL (UNII: 3K9958V90M)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
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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".