NDC 70000-0088 Dry Eye Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70000-0088?
What are the uses for Dry Eye Relief?
Which are Dry Eye Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
Which are Dry Eye Relief 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:
- SODIUM CHLORITE (UNII: G538EBV4VF)
- BORIC ACID (UNII: R57ZHV85D4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MAGNESIUM CHLORATE (UNII: M536P01U3N)
- POTASSIUM CHLORATE (UNII: H35KS68EE7)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Dry Eye Relief?
- RxCUI: 895753 - polyethylene glycol 400 0.4 % / propylene glycol 0.3 % Ophthalmic Gel
- RxCUI: 895753 - polyethylene glycol 400 0.004 MG/MG / propylene glycol 0.003 MG/MG Ophthalmic Gel
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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".