NDC 14222-2003 Soothe Rodan Fields
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 14222-2003?
What are the uses for Soothe Rodan Fields?
Which are Soothe Rodan Fields UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Soothe Rodan Fields 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:
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- CETETH-20 (UNII: I835H2IHHX)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
- TREHALOSE (UNII: B8WCK70T7I)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- PROPYLENE GLYCOL DICAPRYLATE (UNII: 581437HWX2)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Soothe Rodan Fields?
- RxCUI: 103403 - hydrocortisone 1 % Topical Lotion
- RxCUI: 103403 - hydrocortisone 10 MG/ML Topical Lotion
* 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".