NDC 42421-821 Safe Harbor - Natural Sunscreen - Baby And Kids Spf50 Broad Spectrum Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 42421-821?
What are the uses for Safe Harbor - Natural Sunscreen - Baby And Kids Spf50 Broad Spectrum Sunscreen?
Which are Safe Harbor - Natural Sunscreen - Baby And Kids Spf50 Broad Spectrum Sunscreen 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 Sunscreen - Baby And Kids Spf50 Broad Spectrum Sunscreen 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TRICAPRYLIN (UNII: 6P92858988)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TRIMETHOXYCAPRYLYLSILANE (UNII: FZ07E4LW2M)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- PANTHENOL (UNII: WV9CM0O67Z)
- HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J)
- JOJOBA OIL (UNII: 724GKU717M)
- LEVOMENOL (UNII: 24WE03BX2T)
- OAT KERNEL OIL (UNII: 3UVP41R77R)
- ECHINACEA PURPUREA ROOT (UNII: OS64WTR4KU)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- 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".