NDC 62818-101 Acne Solution
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62818 - Biometics Co.,ltd.
- 62818-101 - Acne Solution
Product Packages
NDC Code 62818-101-02
Package Description: 1 BOTTLE in 1 BOX / 40 g in 1 BOTTLE (62818-101-01)
Product Details
What is NDC 62818-101?
Which are Acne Solution 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 Acne Solution 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)
- SAURURUS CHINENSIS WHOLE (UNII: 6DRV3D37XS)
- CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
- BROUSSONETIA PAPYRIFERA WHOLE (UNII: 0QW22BU678)
- MORUS ALBA WHOLE (UNII: C4228R0MX2)
- EUCOMMIA ULMOIDES WHOLE (UNII: 21176878UY)
- PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- LOTUS CORNICULATUS FLOWER VOLATILE OIL (UNII: W11376RO0T)
- CORYLUS AVELLANA POLLEN EXTRACT (UNII: CR2J49TL6L)
- ALLANTOIN (UNII: 344S277G0Z)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CAPSICUM ANNUUM WHOLE (UNII: 7FKZ3QQQ1F)
- ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
- LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)
- CYMBOPOGON MARTINI WHOLE (UNII: 267NPH931L)
- CUPRESSUS SEMPERVIRENS LEAF OIL (UNII: M7QUY89S4O)
What is the NDC to RxNorm Crosswalk for Acne Solution?
- RxCUI: 199308 - salicylic acid 0.5 % Topical Solution
- RxCUI: 199308 - salicylic acid 5 MG/ML Topical Solution
* 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".