NDC 49035-104 Pretty In Paris Hand Sanitizer Bodycology
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49035 - Wal-mart Stores Inc
- 49035-104 - Pretty In Paris Hand Sanitizer
Product Packages
NDC Code 49035-104-02
Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE / 30 mL in 1 BOTTLE, PLASTIC (49035-104-01)
Product Details
What is NDC 49035-104?
What are the uses for Pretty In Paris Hand Sanitizer Bodycology?
Which are Pretty In Paris Hand Sanitizer Bodycology UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Pretty In Paris Hand Sanitizer Bodycology 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)
- TROLAMINE (UNII: 9O3K93S3TK)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- GELATIN (UNII: 2G86QN327L)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Pretty In Paris Hand Sanitizer Bodycology?
- RxCUI: 1047755 - ethanol 75 % Topical Solution
- RxCUI: 1047755 - ethanol 0.75 ML/ML Topical Solution
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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".