NDC 41520-474 Care One Sun Kissed Pear
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41520 - American Sales Company
- 41520-474 - Care One
Product Packages
NDC Code 41520-474-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 41520-474-09
Package Description: 259 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 41520-474?
What are the uses for Care One Sun Kissed Pear?
Which are Care One Sun Kissed Pear UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Care One Sun Kissed 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)
- CARBOMER 934 (UNII: Z135WT9208)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SULISOBENZONE (UNII: 1W6L629B4K)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Care One Sun Kissed Pear?
- RxCUI: 884783 - ethanol 65 % Topical Solution
- RxCUI: 884783 - ethanol 0.65 ML/ML Topical Solution
* 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".