NDC 42352-7001 Solmeet
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42352 - Solbin Co., Ltd
- 42352-7001 - Solmeet
Product Packages
NDC Code 42352-7001-1
Package Description: 120 g in 1 TUBE
Product Details
What is NDC 42352-7001?
What are the uses for Solmeet?
Which are Solmeet UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- AMINOCAPROIC ACID (UNII: U6F3787206)
- AMINOCAPROIC ACID (UNII: U6F3787206) (Active Moiety)
- ALCLOXA (UNII: 18B8O9DQA2)
- ALCLOXA (UNII: 18B8O9DQA2) (Active Moiety)
Which are Solmeet 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XYLITOL (UNII: VCQ006KQ1E)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- PEPPERMINT (UNII: V95R5KMY2B)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)
- ROSIN (UNII: 88S87KL877)
- WATER (UNII: 059QF0KO0R)
* 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".