NDC 11822-3215 Original Redness Reliever
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What is NDC 11822-3215?
What are the uses for Original Redness Reliever?
Which are Original Redness Reliever UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D)
- NAPHAZOLINE (UNII: H231GF11BV) (Active Moiety)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) (Active Moiety)
Which are Original Redness Reliever 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BORIC ACID (UNII: R57ZHV85D4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Original Redness Reliever?
- RxCUI: 1046648 - naphazoline HCl 0.012 % / polyethylene glycol 300 0.2 % Ophthalmic Solution
- RxCUI: 1046648 - naphazoline hydrochloride 0.12 MG/ML / polyethylene glycol 300 2 MG/ML Ophthalmic Solution
- RxCUI: 1046648 - naphazoline hydrochloride 0.012 % / PEG 300 0.2 % Ophthalmic Solution
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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".