NDC 76383-032 Hand Sanitizer Alcohol Free With Lavender Oil Shea Butter
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76383 - Bbc Group Limited
- 76383-032 - Hand Sanitizer
Product Packages
NDC Code 76383-032-03
Package Description: 100 mL in 1 TUBE
Product Details
What is NDC 76383-032?
What are the uses for Hand Sanitizer Alcohol Free With Lavender Oil Shea Butter?
Which are Hand Sanitizer Alcohol Free With Lavender Oil Shea Butter UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Hand Sanitizer Alcohol Free With Lavender Oil Shea Butter 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:
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARETH-25 (UNII: 36ALR4705B)
- PEG-100 STEARATE (UNII: YD01N1999R)
- WATER (UNII: 059QF0KO0R)
- UREA (UNII: 8W8T17847W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SHEA BUTTER (UNII: K49155WL9Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer Alcohol Free With Lavender Oil Shea Butter?
- RxCUI: 1046442 - benzalkonium chloride 0.13 % Topical Lotion
- RxCUI: 1046442 - benzalkonium chloride 1.3 MG/ML Topical Lotion
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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".