NDC 76369-4001 Msm (mosaengmo)
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76369-4001?
What are the uses for Msm (mosaengmo)?
Which are Msm (mosaengmo) UNII Codes?
The UNII codes for the active ingredients in this product are:
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS) (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:
- MENTHOL (UNII: L7T10EIP3A)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COLLAGENASE (UNII: 9X7O8V25IT)
- DIMETHINDENE (UNII: 661FH77Z3P)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CLIMBAZOLE (UNII: 9N42CW7I54)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".