59276-208 NDC - REAL EYEWASH ()

Drug Information

Product NDC: 59276-208

Proprietary Name: Real Eyewash

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	59276-208-12	5 VIAL, SINGLE-USE in 1 BOX (59276-208-12) / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
2	59276-208-14	10 VIAL, SINGLE-USE in 1 BOX (59276-208-14) / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
3	59276-208-16	30 VIAL, SINGLE-USE in 1 BOX (59276-208-16) / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
4	59276-208-18	60 VIAL, SINGLE-USE in 1 BOX (59276-208-18) / 15 mL in 1 VIAL, SINGLE-USE (59276-208-10)
5	59276-208-21	4 VIAL, SINGLE-USE in 1 BOX (59276-208-21) / 30 mL in 1 VIAL, SINGLE-USE (59276-208-20)
6	59276-208-31	1 BOTTLE, PLASTIC in 1 BOX (59276-208-31) / 118 mL in 1 BOTTLE, PLASTIC (59276-208-30)
7	59276-208-41	1 BOTTLE, DISPENSING in 1 BOX (59276-208-41) / 118 mL in 1 BOTTLE, DISPENSING (59276-208-40)
8	59276-208-51	1 BOTTLE, PLASTIC in 1 BOX (59276-208-51) / 148 mL in 1 BOTTLE, PLASTIC (59276-208-50)
9	59276-208-61	1 BOTTLE, PLASTIC in 1 BOX (59276-208-61) / 236 mL in 1 BOTTLE, PLASTIC (59276-208-60)
10	59276-208-71	1 BOTTLE, DISPENSING in 1 BOX (59276-208-71) / 350 mL in 1 BOTTLE, DISPENSING (59276-208-70)
11	59276-208-81	1 BOTTLE, PLASTIC in 1 BOX (59276-208-81) / 474 mL in 1 BOTTLE, PLASTIC (59276-208-80)
12	59276-208-82	2 BOTTLE, PLASTIC in 1 BOX (59276-208-82) / 474 mL in 1 BOTTLE, PLASTIC (59276-208-80)
13	59276-208-91	1 BOTTLE, PLASTIC in 1 BOX (59276-208-91) / 947 mL in 1 BOTTLE, PLASTIC (59276-208-90)
14	59276-208-92	2 BOTTLE, PLASTIC in 1 BOX (59276-208-92) / 947 mL in 1 BOTTLE, PLASTIC (59276-208-90)

Field Name	Field Value	Definition
PRODUCT NDC	59276-208	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	Real Eyewash	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	4/13/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Oliver Landon Intl Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024