NDC 81135-001 Parachute Hand Protect Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81135 - Dbdblab Corp.
- 81135-001 - Parachute Hand Protect Gel
Product Packages
NDC Code 81135-001-02
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 400 mL in 1 BOTTLE, PUMP (81135-001-01)
Product Details
What is NDC 81135-001?
What are the uses for Parachute Hand Protect Gel?
Which are Parachute Hand Protect Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Parachute Hand Protect Gel 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)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- EDETOL (UNII: Q4R969U9FR)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- BETAINE (UNII: 3SCV180C9W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GLYCERIN (UNII: PDC6A3C0OX)
- JUNIPER BERRY OIL (UNII: SZH16H44UY)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- TEA TREE OIL (UNII: VIF565UC2G)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- AZADIRACHTA INDICA LEAF (UNII: HKY915780T)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- CHAMOMILE (UNII: FGL3685T2X)
- MENTHA SUAVEOLENS LEAF (UNII: 1341ZC68MK)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
What is the NDC to RxNorm Crosswalk for Parachute Hand Protect Gel?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
* Please review the disclaimer below.
[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".