NDC 71237-004 Kaewoon For Women
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71237 - Rncare
- 71237-004 - Kaewoon For Women
Product Packages
NDC Code 71237-004-02
Package Description: 1 BOTTLE in 1 CARTON / 320 mL in 1 BOTTLE (71237-004-01)
Product Details
What is NDC 71237-004?
What are the uses for Kaewoon For Women?
Which are Kaewoon For Women UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYALURONIC ACID (UNII: S270N0TRQY)
- HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Kaewoon For Women 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)
- SODIUM COCOATE (UNII: R1TQH25F4I)
- OLEIC ACID (UNII: 2UMI9U37CP)
- COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
- DIGLYCERIN (UNII: 3YC120743U)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYSORBATE 85 (UNII: A7F3N56197)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
- RICE BRAN (UNII: R60QEP13IC)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TURMERIC (UNII: 856YO1Z64F)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- HIPPOPHAE RHAMNOIDES SEED (UNII: ZD5PJT4UZF)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK)
- HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)
- MATRICARIA CHAMOMILLA ROOT (UNII: BTG5H50X7F)
- SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
What is the NDC to RxNorm Crosswalk for Kaewoon For Women?
- RxCUI: 2104187 - allantoin 0.2 % / hyaluronic acid 2 % Medicated Liquid Soap
- RxCUI: 2104187 - allantoin 2 MG/ML / hyaluronic acid 20 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
[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".