NDC 71237-002 Kaewoon
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71237-002?
What are the uses for Kaewoon?
Which are Kaewoon UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Kaewoon 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)
- POTASSIUM COCOATE (UNII: F8U72V8ZXP)
- COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- OLEIC ACID (UNII: 2UMI9U37CP)
- MANDELIC ACID (UNII: NH496X0UJX)
- SPANISH SARDINE (UNII: V837G5YR4R)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- ALLANTOIN (UNII: 344S277G0Z)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIGLYCERIN (UNII: 3YC120743U)
- RICE BRAN (UNII: R60QEP13IC)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- MUNG BEAN (UNII: 1LIB31N73G)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)
- POLYSORBATE 85 (UNII: A7F3N56197)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYL/CAPRAMIDOPROPYL BETAINE (UNII: 231H3ZT9NE)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
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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".