NDC 49738-413 Little Ones Baby Fresh Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49738 - Kmart Corporation
- 49738-413 - Little Ones
Product Packages
NDC Code 49738-413-02
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 49738-413-03
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 49738-413-07
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 49738-413-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 49738-413-32
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 49738-413-33
Package Description: 946 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 49738-413?
What are the uses for Little Ones Baby Fresh Sanitizer?
Which are Little Ones Baby Fresh Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Little Ones Baby Fresh Sanitizer 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)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Little Ones Baby Fresh Sanitizer?
- 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".