NDC 59276-208 Real Eyewash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 59276-208-12
Package Description: 5 VIAL, SINGLE-USE in 1 BOX / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
NDC Code 59276-208-14
Package Description: 10 VIAL, SINGLE-USE in 1 BOX / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
NDC Code 59276-208-16
Package Description: 30 VIAL, SINGLE-USE in 1 BOX / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
NDC Code 59276-208-18
Package Description: 60 VIAL, SINGLE-USE in 1 BOX / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
NDC Code 59276-208-21
Package Description: 4 VIAL, SINGLE-USE in 1 BOX / 30 mL in 1 VIAL, SINGLE-USE (59276-208-20)
NDC Code 59276-208-31
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 118 mL in 1 BOTTLE, PLASTIC (59276-208-30)
NDC Code 59276-208-41
Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 118 mL in 1 BOTTLE, DISPENSING (59276-208-40)
NDC Code 59276-208-51
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 148 mL in 1 BOTTLE, PLASTIC (59276-208-50)
NDC Code 59276-208-61
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 236 mL in 1 BOTTLE, PLASTIC (59276-208-60)
NDC Code 59276-208-71
Package Description: 1 BOTTLE, DISPENSING in 1 BOX / 350 mL in 1 BOTTLE, DISPENSING (59276-208-70)
NDC Code 59276-208-81
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 474 mL in 1 BOTTLE, PLASTIC (59276-208-80)
NDC Code 59276-208-82
Package Description: 2 BOTTLE, PLASTIC in 1 BOX / 474 mL in 1 BOTTLE, PLASTIC (59276-208-80)
NDC Code 59276-208-91
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 947 mL in 1 BOTTLE, PLASTIC (59276-208-90)
NDC Code 59276-208-92
Package Description: 2 BOTTLE, PLASTIC in 1 BOX / 947 mL in 1 BOTTLE, PLASTIC (59276-208-90)
Product Details
What is NDC 59276-208?
What are the uses for Real Eyewash?
Which are Real Eyewash UNII Codes?
The UNII codes for the active ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
Which are Real Eyewash 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:
- POLIHEXANIDE (UNII: 322U039GMF)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM PHOSPHATE, DIBASIC, DODECAHYDRATE (UNII: E1W4N241FO)
- SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Real Eyewash?
- RxCUI: 1053173 - water 98.6 % Ophthalmic Irrigation Solution
- RxCUI: 1053173 - water 986 MG/ML Ophthalmic Irrigation Solution
- RxCUI: 1053173 - water 98.577 % Ophthalmic Irrigation Solution
- RxCUI: 1053173 - water 98.6 ML per 100 ML Ophthalmic Irrigation 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".