NDC 11822-4650 Pure Spring
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-4650 - Pure Spring
Product Packages
NDC Code 11822-4650-9
Package Description: 260 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11822-4650?
What are the uses for Pure Spring?
Which are Pure Spring UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Pure 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- CARBOMER 934 (UNII: Z135WT9208)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MANNITOL (UNII: 3OWL53L36A)
- ALPHA CELLULOSE (UNII: I355QGZ19A)
- HYPROMELLOSE 2208 (4000 MPA.S) (UNII: 39J80LT57T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CARAMEL (UNII: T9D99G2B1R)
What is the NDC to RxNorm Crosswalk for Pure Spring?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 ML/ML Topical 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".