NDC 62032-124 Nu-derm Sun Shield Spf 50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62032 - Omp, Inc.
- 62032-124 - Nu-derm Sun Shield Spf 50 Sunscreen
Product Characteristics
Product Packages
NDC Code 62032-124-10
Package Description: 1 TUBE in 1 CARTON / 89 mL in 1 TUBE
Product Details
What is NDC 62032-124?
What are the uses for Nu-derm Sun Shield Spf 50 Sunscreen?
Which are Nu-derm Sun Shield Spf 50 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Nu-derm Sun Shield Spf 50 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- WATER (UNII: 059QF0KO0R)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TROPOLONE (UNII: 7L6DL16P1T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- UBIDECARENONE (UNII: EJ27X76M46)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
* Please review the disclaimer below.
[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".