NDC 72197-016 Pharmacys Prescription 4.5 Oz Creamy Petroleum Jelly
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72197 - American Consumer Products Corp
- 72197-016 - Pharmacys Prescription 4.5 Oz Creamy Petroleum Jelly
Product Packages
NDC Code 72197-016-04
Package Description: 127.57 g in 1 TUBE
Product Details
What is NDC 72197-016?
What are the uses for Pharmacys Prescription 4.5 Oz Creamy Petroleum Jelly?
Which are Pharmacys Prescription 4.5 Oz Creamy Petroleum Jelly UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Pharmacys Prescription 4.5 Oz Creamy Petroleum Jelly 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAURETH-20 (UNII: 6SU0SC83AH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MINERAL OIL (UNII: T5L8T28FGP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Pharmacys Prescription 4.5 Oz Creamy Petroleum Jelly?
- RxCUI: 1037285 - petrolatum 30 % Topical Gel
- RxCUI: 1037285 - petrolatum 0.3 MG/MG Topical Gel
- RxCUI: 1037285 - petrolatum 30 % Topical Jelly
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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".