NDC 71825-102 Cremo Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71825 - Cremo Company
- 71825-102 - Cremo Sunscreen
Product Packages
NDC Code 71825-102-01
Package Description: 59 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 71825-102?
What are the uses for Cremo Sunscreen?
Which are Cremo Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Cremo 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- WATER (UNII: 059QF0KO0R)
- SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POMEGRANATE (UNII: 56687D1Z4D)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER 940 (UNII: 4Q93RCW27E)
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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".