NDC 11822-8071 Rite Aid Renewal Clear Spring
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid Corporation
- 11822-8071 - Rite Aid Renewal
Product Packages
NDC Code 11822-8071-8
Package Description: 532 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11822-8071?
What are the uses for Rite Aid Renewal Clear Spring?
Which are Rite Aid Renewal Clear Spring 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 Clear Spring 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)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE (UNII: 082Y3WQI5K)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE (UNII: 205Z54J075)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Rite Aid Renewal Clear Spring?
- RxCUI: 1020118 - triclosan 0.15 % Medicated Liquid Soap
- RxCUI: 1020118 - triclosan 1.5 MG/ML Medicated Liquid Soap
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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".