NDC 73022-005 Mineral Sunscreen Spf 30 For Kids And Babies Boo Bamboo
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 73022-005?
What are the uses for Mineral Sunscreen Spf 30 For Kids And Babies Boo Bamboo?
Which are Mineral Sunscreen Spf 30 For Kids And Babies Boo Bamboo 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 Mineral Sunscreen Spf 30 For Kids And Babies Boo Bamboo 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- BAMBUSA BAMBOS STEM (UNII: NRA4497HC5)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- DILAURYL CITRATE (UNII: 5OYS3G306B)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- LONICERA CONFUSA FLOWER (UNII: 3JV904IJ0V)
- METHYLCELLULOSE (15 MPA.S) (UNII: NPU9M2E6L8)
- OCTYLDODECYL STEARATE (UNII: K6F16QGO28)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYGLYCERYL-3 LAURATE (UNII: Y9ZSR39D0E)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)
- JOJOBA OIL (UNII: 724GKU717M)
- SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- TOCOPHEROL (UNII: R0ZB2556P8)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".