NDC 64942-1038 Vaseline Intensive Rescue Clinical Therapy Fragrance Free
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco Inc. D/b/a Unilever
- 64942-1038 - Vaseline
Product Packages
NDC Code 64942-1038-2
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 200 mL in 1 BOTTLE, PLASTIC (64942-1038-1)
NDC Code 64942-1038-3
Package Description: 50 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 64942-1038?
What are the uses for Vaseline Intensive Rescue Clinical Therapy Fragrance Free?
Which are Vaseline Intensive Rescue Clinical Therapy Fragrance Free UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Vaseline Intensive Rescue Clinical Therapy Fragrance Free 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)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MINERAL OIL (UNII: T5L8T28FGP)
- STEARETH-21 (UNII: 53J3F32P58)
- BORAGO OFFICINALIS SEED (UNII: 2GXJ790US0)
- PETROLATUM (UNII: 4T6H12BN9U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- STEARYL STEARATE (UNII: 5WX2EGD0DK)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLENIC ACID (UNII: 0RBV727H71)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Vaseline Intensive Rescue Clinical Therapy Fragrance Free?
- RxCUI: 199680 - dimethicone 1 % Topical Lotion
- RxCUI: 199680 - dimethicone 10 MG/ML Topical Lotion
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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".