NDC 43948-1201 Ac Out Spot Stop Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43948 - The Doctors Cosmetics Co., Ltd
- 43948-1201 - Ac Out Spot Stop Serum
Product Packages
NDC Code 43948-1201-1
Package Description: 15 mL in 1 TUBE
Product Details
What is NDC 43948-1201?
What are the uses for Ac Out Spot Stop Serum?
Which are Ac Out Spot Stop Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Ac Out Spot Stop Serum 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:
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CHRYSANTHEMUM X MORIFOLIUM FLOWER (UNII: 2GR3C1A0WV)
- MAGNOLIA KOBUS BARK (UNII: 54LVP49595)
- THUJOPSIS DOLABRATA LEAFY TWIG (UNII: P24JH909CP)
- PUMMELO (UNII: ET1TN5W71X)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
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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".