NDC 11822-1120 Rite Aid Renewal Pear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid Corporation
- 11822-1120 - Rite Aid Renewal
Product Packages
NDC Code 11822-1120-8
Package Description: 221 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11822-1120?
What are the uses for Rite Aid Renewal Pear?
Which are Rite Aid Renewal Pear UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Rite Aid Renewal Pear 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Rite Aid Renewal Pear?
- RxCUI: 1053855 - triclosan 0.46 % Medicated Liquid Soap
- RxCUI: 1053855 - triclosan 4.6 MG/ML Medicated Liquid Soap
- RxCUI: 1053855 - triclosan 0.46 % Foaming Medicated Hand Soap
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Patient Education
Pseudoephedrine
Pseudoephedrine is used to relieve nasal congestion caused by colds, allergies, and hay fever. It is also used to temporarily relieve sinus congestion and pressure. Pseudoephedrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Pseudoephedrine is in a class of medications called nasal decongestants. It works by causing narrowing of the blood vessels in the nasal passages.
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* 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".