NDC 0699-5743 Moist Sure
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 0699-5743?
What are the uses for Moist Sure?
Which are Moist Sure UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Moist Sure 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)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- SORBITOL (UNII: 506T60A25R)
- ETHANOLAMINE (UNII: 5KV86114PT)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
What is the NDC to RxNorm Crosswalk for Moist Sure?
- RxCUI: 1042637 - isopropyl alcohol 63 % Topical Solution
- RxCUI: 1042637 - isopropyl alcohol 0.63 ML/ML Topical Solution
- RxCUI: 616763 - ethanol 62 % Topical Foam
- RxCUI: 616763 - ethanol 0.62 ML/ML Topical Foam
* 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".