NDC 73192-030 People4ocean Spf50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73192 - P4o Distribution Pty Ltd
- 73192-030 - People4ocean Spf50 Sunscreen
Product Packages
NDC Code 73192-030-00
Package Description: 1000 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 73192-030?
What are the uses for People4ocean Spf50 Sunscreen?
Which are People4ocean Spf50 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are People4ocean Spf50 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:
- PEG-30 DIPOLYHYDROXYSTEARATE (4000 MW) (UNII: 9713Q0S7FO)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERIN (UNII: PDC6A3C0OX)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CANANGA OIL (UNII: 8YOY78GNNX)
- GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
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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".