NDC 70000-0090 Lubricant Drops
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70000 - Cardinal Health, 110 Dba Leader
- 70000-0090 - Lubricant Drops
Product Packages
NDC Code 70000-0090-1
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 15 mL in 1 BOTTLE, DROPPER
Price per Unit: $0.49767 per ML
NDC Code 70000-0090-2
Package Description: 2 BOTTLE, DROPPER in 1 CARTON / 15 mL in 1 BOTTLE, DROPPER
Price per Unit: $0.29200 per ML
Product Details
What is NDC 70000-0090?
What are the uses for Lubricant Drops?
Which are Lubricant Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)
Which are Lubricant Drops 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:
- BORIC ACID (UNII: R57ZHV85D4)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORITE (UNII: G538EBV4VF)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Lubricant Drops?
- 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".