NDC 11673-636 Up And Up Lubricant Refreshing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11673 - Target Corporation
- 11673-636 - Up And Up Lubricant Refreshing
Product Packages
NDC Code 11673-636-70
Package Description: 70 VIAL in 1 CARTON / .4 mL in 1 VIAL
Product Details
What is NDC 11673-636?
What are the uses for Up And Up Lubricant Refreshing?
Which are Up And Up Lubricant Refreshing UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)
Which are Up And Up Lubricant Refreshing 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:
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Up And Up Lubricant Refreshing?
- RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
- RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
- RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic 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".