NDC 44781-200 Esopinio Jewel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 44781 - Zion Synthetic Fiber Co., Ltd.
- 44781-200 - Esopinio Jewel
Product Packages
NDC Code 44781-200-01
Package Description: 120 g in 1 CARTON
Product Details
What is NDC 44781-200?
What are the uses for Esopinio Jewel?
Which are Esopinio Jewel UNII Codes?
The UNII codes for the active ingredients in this product are:
- WITCH HAZEL (UNII: 101I4J0U34)
- WITCH HAZEL (UNII: 101I4J0U34) (Active Moiety)
Which are Esopinio Jewel 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)
- ALUMINUM SILICATE (UNII: T1FAD4SS2M)
- SHEA BUTTER (UNII: K49155WL9Y)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- COCONUT (UNII: 3RT3536DHY)
- PALM KERNEL OIL (UNII: B0S90M0233)
- SQUALANE (UNII: GW89575KF9)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WINE GRAPE (UNII: 3GOV20705G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- APRICOT (UNII: 269CJD5GZ9)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HONEY (UNII: Y9H1V576FH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE FEROX LEAF (UNII: 0D145J8EME)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
What is the NDC to RxNorm Crosswalk for Esopinio Jewel?
- RxCUI: 1151061 - witch hazel 0.1 % Medicated Bar Soap
- RxCUI: 1151061 - witch hazel 0.001 MG/MG Medicated Bar 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".