NDC 70840-001 White And Elm Everyday Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70840-001?
Which are White And Elm Everyday Spf 15 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 White And Elm Everyday Spf 15 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:
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALOE (UNII: V5VD430YW9)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
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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".