NDC 11822-0317 Rite Aid Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-0317 - Rite Aid
Product Characteristics
Product Packages
NDC Code 11822-0317-9
Package Description: 1 TUBE in 1 CARTON / 11.9 g in 1 TUBE (11822-0317-2)
Product Details
What is NDC 11822-0317?
What are the uses for Rite Aid Maximum Strength?
Which are Rite Aid Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Rite Aid Maximum Strength 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:
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBIC ACID (UNII: X045WJ989B)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALLANTOIN (UNII: 344S277G0Z)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- PEPPERMINT OIL (UNII: AV092KU4JH)
* 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".