NDC 64942-0276 Vaseline Petroleum Jelly Deep Moisture
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco Inc. D/b/a Unilever
- 64942-0276 - Vaseline
Product Packages
NDC Code 64942-0276-1
Package Description: 127 g in 1 TUBE
Product Details
What is NDC 64942-0276?
What are the uses for Vaseline Petroleum Jelly Deep Moisture?
Which are Vaseline Petroleum Jelly Deep Moisture UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Vaseline Petroleum Jelly Deep Moisture 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Vaseline Petroleum Jelly Deep Moisture?
- RxCUI: 1043075 - petrolatum 30 % Topical Cream
- RxCUI: 1043075 - petrolatum 300 MG/ML Topical Cream
- RxCUI: 1045489 - Vaseline 30 % Topical Cream
- RxCUI: 1045489 - petrolatum 300 MG/ML Topical Cream [Vaseline]
- RxCUI: 1045489 - Vaseline 300 MG/ML Topical Cream
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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".