NDC 71630-173 Doterra Sun
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71630-173?
What are the uses for Doterra Sun?
Which are Doterra Sun UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Doterra Sun 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:
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- YLANG-YLANG OIL (UNII: 8YOY78GNNX)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BUTYLOCTANOL (UNII: N442D9VO79)
- SQUALENE (UNII: 7QWM220FJH)
- MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN)
- EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
- TURMERIC OIL (UNII: 6KGS8SP16U)
- HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)
- PROPANEDIOL (UNII: 5965N8W85T)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
- BENTONITE (UNII: A3N5ZCN45C)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- .BETA.-BISABOLOL (UNII: LP618AV2EA)
- MANDARIN OIL (UNII: NJO720F72R)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- COCO GLUCOSIDE (UNII: ICS790225B)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- COCONUT (UNII: 3RT3536DHY)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- WATER (UNII: 059QF0KO0R)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- CARROT SEED OIL (UNII: 595AO13F11)
- MALIC ACID (UNII: 817L1N4CKP)
* 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".