NDC 75410-001 Story Of Love Instant Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75410 - Yiwu Story Of Love Cosmetic Co., Ltd
- 75410-001 - Story Of Love Instant Hand Sanitizer
Product Packages
NDC Code 75410-001-01
Package Description: 250 mL in 1 BOTTLE
NDC Code 75410-001-02
Package Description: 20 mL in 1 BOTTLE
NDC Code 75410-001-03
Package Description: 30 mL in 1 BOTTLE
NDC Code 75410-001-04
Package Description: 60 mL in 1 BOTTLE
NDC Code 75410-001-05
Package Description: 237 mL in 1 BOTTLE
NDC Code 75410-001-06
Package Description: 240 mL in 1 BOTTLE
NDC Code 75410-001-07
Package Description: 500 mL in 1 BOTTLE
NDC Code 75410-001-08
Package Description: 1000 mL in 1 BOTTLE
NDC Code 75410-001-09
Package Description: 100 mL in 1 BOTTLE
NDC Code 75410-001-10
Package Description: 300 mL in 1 BOTTLE
Product Details
What is NDC 75410-001?
What are the uses for Story Of Love Instant Hand Sanitizer?
Which are Story Of Love Instant Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Story Of Love Instant Hand 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER 934 (UNII: Z135WT9208)
- TRIETHANOLAMINE SULFATE (UNII: MV1V89M17O)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
What is the NDC to RxNorm Crosswalk for Story Of Love Instant Hand Sanitizer?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 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".