NDC 58133-652 Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58133 - Cosmetic Specialty Labs, Inc.
- 58133-652 - Spf30
Product Characteristics
Product Packages
NDC Code 58133-652-33
Package Description: 100 mL in 1 TUBE
NDC Code 58133-652-35
Package Description: 100 mL in 1 TUBE
NDC Code 58133-652-36
Package Description: 100 mL in 1 TUBE
Product Details
What is NDC 58133-652?
What are the uses for Spf30?
Which are Spf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Spf30 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- COCONUT OIL (UNII: Q9L0O73W7L)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CHAMOMILE (UNII: FGL3685T2X)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SHEA BUTTER (UNII: K49155WL9Y)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CANDELILLA WAX (UNII: WL0328HX19)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COMFREY (UNII: D05HXK6R3G)
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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".