NDC 54948-110 Baeknyondongan Chi
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54948-110?
What are the uses for Baeknyondongan Chi?
Which are Baeknyondongan Chi 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 Baeknyondongan Chi 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:
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- WATER (UNII: 059QF0KO0R)
- PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
- TROLAMINE (UNII: 9O3K93S3TK)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MENTHOL (UNII: L7T10EIP3A)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PRUNUS ARMENIACA SEED (UNII: 75356789IW)
- PRUNUS PERSICA SEED (UNII: V9C81470RR)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)
What is the NDC to RxNorm Crosswalk for Baeknyondongan Chi?
- RxCUI: 1297242 - witch hazel 0.1 % Medicated Shampoo
- RxCUI: 1297242 - witch hazel 1 MG/ML Medicated Shampoo
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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".