NDC 51220-4001 Cheon Shim Bo Yun
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51220 - Saimdang Cosmetics Co., Ltd
- 51220-4001 - Cheon Shim Bo Yun
Product Characteristics
Product Packages
NDC Code 51220-4001-1
Package Description: 112 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 51220-4001?
What are the uses for Cheon Shim Bo Yun?
Which are Cheon Shim Bo Yun UNII Codes?
The UNII codes for the active ingredients in this product are:
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
- N-ACETYLGLUCOSAMINE (UNII: V956696549) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) (Active Moiety)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- SOY ISOFLAVONES (UNII: 71B37NR06D) (Active Moiety)
Which are Cheon Shim Bo Yun 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:
- SOYBEAN OIL (UNII: 241ATL177A)
- WHEAT GERM OIL (UNII: 14C97E680P)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CALCIUM (UNII: SY7Q814VUP)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- POMEGRANATE (UNII: 56687D1Z4D)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- COCHINEAL (UNII: TZ8Z31B35M)
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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".