NDC 76261-127 Hydrating Lip Balm Spf 15 Sunscreen Asap
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76261 - Australian Skin Products Pty Ltd
- 76261-127 - Hydrating Lip Balm Spf 15 Sunscreen
Product Packages
NDC Code 76261-127-02
Package Description: 1 TUBE in 1 CARTON / 10 mL in 1 TUBE (76261-127-01)
Product Details
What is NDC 76261-127?
What are the uses for Hydrating Lip Balm Spf 15 Sunscreen Asap?
Which are Hydrating Lip Balm Spf 15 Sunscreen Asap UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Hydrating Lip Balm Spf 15 Sunscreen Asap 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:
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- NIACINAMIDE (UNII: 25X51I8RD4)
- TRICAPRYLIN (UNII: 6P92858988)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- TOCOPHEROL (UNII: R0ZB2556P8)
- GINGER (UNII: C5529G5JPQ)
- MALIC ACID (UNII: 817L1N4CKP)
- MANDARIN OIL (UNII: NJO720F72R)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- LEMON OIL (UNII: I9GRO824LL)
- ETHYL METHYLPHENYLGLYCIDATE (UNII: UD51D5KR4A)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
* Please review the disclaimer below.
[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".