NDC 71502-002 Uniwell Natural Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71502 - Uniwell Ltd
- 71502-002 - Uniwell Natural Essence
Product Packages
NDC Code 71502-002-02
Package Description: 1 CONTAINER in 1 PACKAGE / 50 mL in 1 CONTAINER (71502-002-01)
Product Details
What is NDC 71502-002?
What are the uses for Uniwell Natural Essence?
Which are Uniwell Natural Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Uniwell Natural Essence 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- NIACINAMIDE (UNII: 25X51I8RD4)
- SQUALANE (UNII: GW89575KF9)
- ARGININE (UNII: 94ZLA3W45F)
- PROPANEDIOL (UNII: 5965N8W85T)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- 2-HYDROXYACETOPHENONE (UNII: DQ1N9R01IA)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- ORANGE OIL (UNII: AKN3KSD11B)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ADENOSINE (UNII: K72T3FS567)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- COCOA (UNII: D9108TZ9KG)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ECKLONIA CAVA (UNII: UXX2N5V39P)
- SOYBEAN (UNII: L7HT8F1ZOD)
- WHEAT SPROUT (UNII: 3K32950CI0)
- BROCCOLI SPROUT (UNII: 128UH9LOAE)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- MAGNOLIA LILIIFLORA FLOWER (UNII: SVM28292LH)
- CLOVE (UNII: K48IKT5321)
- STYPHNOLOBIUM JAPONICUM FLOWER (UNII: 644C3CSB6E)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LEMON OIL (UNII: I9GRO824LL)
- ALCOHOL (UNII: 3K9958V90M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
* 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".