NDC 68973-002 Renuee
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68973 - Pmc Trade, Export And Import
- 68973-002 - Renuee
Product Packages
NDC Code 68973-002-90
Package Description: 90 g in 1 TUBE
Product Details
What is NDC 68973-002?
What are the uses for Renuee?
Which are Renuee UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Renuee 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- GINKGO BILOBA WHOLE (UNII: 660486U6OI)
- SHEA BUTTER (UNII: K49155WL9Y)
- CAFFEINE (UNII: 3G6A5W338E)
- ALMOND OIL (UNII: 66YXD4DKO9)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
- JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
- GLYCERIN (UNII: PDC6A3C0OX)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- D&C ORANGE NO. 11 (UNII: B16H36W4W4)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Renuee?
- RxCUI: 1544377 - Renuee 2 % Topical Cream
- RxCUI: 1544377 - dimethicone 20 MG/ML Topical Cream [Renuee]
- RxCUI: 1544377 - Renuee 20 MG/ML Topical Cream
- RxCUI: 244642 - dimethicone 2 % Topical Cream
- RxCUI: 244642 - dimethicone 20 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".