NDC 42421-575 Safe Harbor Natural Suncare Broad Spectrum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42421 - Emilia Personal Care Inc
- 42421-575 - Safe Harbor Natural Suncare
Product Packages
NDC Code 42421-575-15
Package Description: 124 g in 1 TUBE
Product Details
What is NDC 42421-575?
What are the uses for Safe Harbor Natural Suncare Broad Spectrum?
Which are Safe Harbor Natural Suncare Broad Spectrum UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Safe Harbor Natural Suncare Broad Spectrum 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SESAME OIL (UNII: QX10HYY4QV)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- JOJOBA OIL (UNII: 724GKU717M)
- GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
- SHEA BUTTER (UNII: K49155WL9Y)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- TRIMETHOXYCAPRYLYLSILANE (UNII: FZ07E4LW2M)
- ALLANTOIN (UNII: 344S277G0Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- LEVOMENOL (UNII: 24WE03BX2T)
- HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
- OAT (UNII: Z6J799EAJK)
- ECHINACEA PURPUREA ROOT (UNII: OS64WTR4KU)
- MATRICARIA RECUTITA ROOT (UNII: BTG5H50X7F)
- TILIA X EUROPAEA FLOWER (UNII: NHV2K1OUDH)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
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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".