NDC 77371-010 Shower Pouch Unscented
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77371 - Nicety Solutions Llc
- 77371-010 - Shower Pouch Unscented
Product Packages
NDC Code 77371-010-01
Package Description: 54 mL in 1 PACKET
Product Details
What is NDC 77371-010?
What are the uses for Shower Pouch Unscented?
Which are Shower Pouch Unscented UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Shower Pouch Unscented 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:
- ALCOHOL (UNII: 3K9958V90M)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- TEA TREE OIL (UNII: VIF565UC2G)
- MENTHOL (UNII: L7T10EIP3A)
- WILLOW BARK (UNII: S883J9JDYX)
- PANTHENOL (UNII: WV9CM0O67Z)
- WITCH HAZEL (UNII: 101I4J0U34)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TRIMETHYLENEDIAMINETETRAACETIC ACID (UNII: 3F6OA94EER)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Shower Pouch Unscented?
- RxCUI: 2287160 - isopropyl alcohol 75 % Medicated Pad
- RxCUI: 2287160 - isopropyl alcohol 0.75 ML/ML Medicated Pad
- RxCUI: 2287160 - isopropyl alcohol 75 % Topical Cloth
- RxCUI: 2287160 - isopropyl alcohol 75 % Topical Swab
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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".