NDC 70708-020 Gurunanda Hand Sanitizer Grapefruit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70708 - Gurunanda, Llc
- 70708-020 - Gurunanda Hand Sanitizer
Product Characteristics
Product Packages
NDC Code 70708-020-01
Package Description: 60 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 70708-020?
What are the uses for Gurunanda Hand Sanitizer Grapefruit?
Which are Gurunanda Hand Sanitizer Grapefruit 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 Gurunanda Hand Sanitizer Grapefruit 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:
- COCONUT OIL (UNII: Q9L0O73W7L)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- BITTER ORANGE OIL (UNII: 9TLV70SV6I)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- DEANOL (UNII: 2N6K9DRA24)
- VANILLA PLANIFOLIA OIL (UNII: 0A3F415158)
- EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
- LIME OIL (UNII: UZH29XGA8G)
- ORANGE OIL (UNII: AKN3KSD11B)
- WATER (UNII: 059QF0KO0R)
- CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
- LEMON OIL (UNII: I9GRO824LL)
What is the NDC to RxNorm Crosswalk for Gurunanda Hand Sanitizer Grapefruit?
- RxCUI: 1014638 - isopropyl alcohol 70 % Topical Spray
- RxCUI: 1014638 - isopropyl alcohol 0.7 ML/ML Topical Spray
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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".