NDC 53208-377 Gongjinhyang Seol Whitening Jinaek Program
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-377 - Gongjinhyang Seol Whitening Jinaek Program
Product Packages
NDC Code 53208-377-02
Package Description: 1 CONTAINER in 1 BOX / 45 mL in 1 CONTAINER (53208-377-01)
Product Details
What is NDC 53208-377?
Which are Gongjinhyang Seol Whitening Jinaek Program UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIACETYL BENZOYL LATHYROL (UNII: 8986760I2S)
- DIACETYL BENZOYL LATHYROL (UNII: 8986760I2S) (Active Moiety)
Which are Gongjinhyang Seol Whitening Jinaek Program 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)
- CAPRYLIC/CAPRIC MONO/DIGLYCERIDES (UNII: U72Q2I8C85)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- 2-ETHYLHEXANOIC ACID (UNII: 01MU2J7VVZ)
- PANTHENOL (UNII: WV9CM0O67Z)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SQUALANE (UNII: GW89575KF9)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- MORUS ALBA ROOT BARK (UNII: SV6B76DK9N)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- N-ACETYL-TYROSINE (UNII: DA8G610ZO5)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- DIOSMETIN (UNII: TWZ37241OT)
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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".