NDC 69423-603 First Aid Beauty Fab Broad Spectrum Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69423 - The Procter & Gamble Manufacturing Company
- 69423-603 - First Aid Beauty Fab Broad Spectrum Sunscreen Spf 30
Product Packages
NDC Code 69423-603-50
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69423-603?
What are the uses for First Aid Beauty Fab Broad Spectrum Sunscreen Spf 30?
Which are First Aid Beauty Fab Broad Spectrum Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are First Aid Beauty Fab Broad Spectrum Sunscreen Spf 30 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:
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALPHA-ARBUTIN (UNII: 72VUP07IT5)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- TANACETUM PARTHENIUM (UNII: 6GE7Z0761K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COPAIFERA OFFICINALIS RESIN (UNII: 1VH544O5AT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ULVA COMPRESSA (UNII: SXZ209FM33)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENYL METHICONE (500 CST) (UNII: 5T0F958X3Z)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- 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".