NDC 69994-001 Biolle Tears
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 69994-001-02
Package Description: 2 VIAL, SINGLE-USE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-USE
NDC Code 69994-001-04
Package Description: 4 VIAL, SINGLE-USE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-USE
NDC Code 69994-001-10
Package Description: 102 VIAL, SINGLE-USE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-USE
NDC Code 69994-001-32
Package Description: 32 VIAL, SINGLE-USE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-USE
NDC Code 69994-001-52
Package Description: 52 VIAL, SINGLE-USE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-USE
NDC Code 69994-001-72
Package Description: 72 VIAL, SINGLE-USE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-USE
Product Details
What is NDC 69994-001?
What are the uses for Biolle Tears?
Which are Biolle Tears UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)
Which are Biolle Tears 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)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Biolle Tears?
- 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
- RxCUI: 1745014 - Biolle Tears 0.5 % Ophthalmic Solution
- RxCUI: 1745014 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution [Biolle Tears]
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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".