NDC 0573-0728 Chapstick Moisturizer Green Apple
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0573 - Glaxosmithkline Consumer Healthcare Holdings (us) Llc
- 0573-0728 - Chapstick Moisturizer Green Apple
Product Characteristics
Product Packages
NDC Code 0573-0728-12
Package Description: 1 CYLINDER in 1 BLISTER PACK / 4 g in 1 CYLINDER
NDC Code 0573-0728-40
Package Description: 3 CYLINDER in 1 BLISTER PACK / 4 g in 1 CYLINDER
NDC Code 0573-0728-51
Package Description: 4 g in 1 CYLINDER
Product Details
What is NDC 0573-0728?
What are the uses for Chapstick Moisturizer Green Apple?
Which are Chapstick Moisturizer Green Apple UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Chapstick Moisturizer Green Apple 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- .ALPHA.-TOCOPHEROL LINOLEATE, D- (UNII: G0N132Q0ED)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- LANOLIN (UNII: 7EV65EAW6H)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MINERAL OIL (UNII: T5L8T28FGP)
- PARAFFIN (UNII: I9O0E3H2ZE)
- SACCHARIN (UNII: FST467XS7D)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WHITE WAX (UNII: 7G1J5DA97F)
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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".