NDC 72667-007 Rocky Mountain Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72667 - Inspec Solutions Llc.
- 72667-007 - Rocky Mountain Spf 30
Product Packages
NDC Code 72667-007-01
Package Description: 3785 g in 1 BOTTLE, PLASTIC
NDC Code 72667-007-02
Package Description: 806 g in 1 BOTTLE, PLASTIC
NDC Code 72667-007-03
Package Description: 180 g in 1 BOTTLE, PLASTIC
NDC Code 72667-007-04
Package Description: 59 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 72667-007?
What are the uses for Rocky Mountain Spf 30?
Which are Rocky Mountain Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Rocky Mountain 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:
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CARBOMER 934 (UNII: Z135WT9208)
- TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE (UNII: N2TK31JIAH)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- .ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOL HYDROCHLORIDE, ERYTHRO-(+/-)- (UNII: 3IIJ9C722I)
- TOCOPHEROL (UNII: R0ZB2556P8)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE 500 (UNII: 5L1VVC3K8O)
- STEARIC ACID D7 (UNII: T3B081197X)
- SORBITOL (UNII: 506T60A25R)
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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".