NDC 76369-3001 Msm (mosaengmo)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 76369-3001?
What are the uses for Msm (mosaengmo)?
Which are Msm (mosaengmo) UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
Which are Msm (mosaengmo) 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)
- WATER (UNII: 059QF0KO0R)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- DIOXYBENZONE (UNII: B762XZ551X)
- NIACINAMIDE (UNII: 25X51I8RD4)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
- PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- GARLIC (UNII: V1V998DC17)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
- ROSEMARY (UNII: IJ67X351P9)
- LAMIUM ALBUM FLOWER (UNII: 62IB9494JA)
- POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM)
* 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".