NDC 70365-001 Aubio Life Sciences Lip
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70365 - Aubio Life Sciences Llc
- 70365-001 - Aubio Life Sciences Lip
Product Packages
NDC Code 70365-001-01
Package Description: 3 g in 1 BLISTER PACK
Product Details
What is NDC 70365-001?
What are the uses for Aubio Life Sciences Lip?
Which are Aubio Life Sciences Lip UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Aubio Life Sciences Lip 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLIC ALCOHOL (UNII: NV1779205D)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CERAMIDE NP (UNII: 4370DF050B)
- 3-DEHYDROXY CERAMIDE 1 (UNII: CR0J8RN66K)
- CERAMIDE AP (UNII: F1X8L2B00J)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- MELISSA OFFICINALIS (UNII: YF70189L0N)
- SARRACENIA PURPUREA (UNII: FOP08H143P)
What is the NDC to RxNorm Crosswalk for Aubio Life Sciences Lip?
- RxCUI: 1739846 - allantoin 0.5 % / lidocaine 0.5 % Topical Cream
- RxCUI: 1739846 - allantoin 5 MG/ML / lidocaine 5 MG/ML Topical Cream
* 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".