NDC 58892-125 Lipcotz Lip Balm/sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58892-125?
What are the uses for Lipcotz Lip Balm/sunscreen?
Which are Lipcotz Lip Balm/sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Lipcotz Lip Balm/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:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CERESIN (UNII: Q1LS2UJO3A)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- KIWI FRUIT (UNII: 71ES77LGJC)
- LIME (CITRUS) (UNII: 8CZS546954)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HEXYLDECANOL (UNII: 151Z7P1317)
- HEXYLDECYL LAURATE (UNII: 0V595C1P6M)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- GINGER OIL (UNII: SAS9Z1SVUK)
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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".