NDC 14222-1615 Skin Lightening Rodan Fields
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14222 - Rodan & Fields, Llc.
- 14222-1615 - Skin Lightening
Product Packages
NDC Code 14222-1615-2
Package Description: 1 TUBE in 1 BOX / 125 mL in 1 TUBE (14222-1615-1)
Product Details
What is NDC 14222-1615?
What are the uses for Skin Lightening Rodan Fields?
Which are Skin Lightening Rodan Fields UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Skin Lightening 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:
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- WITCH HAZEL (UNII: 101I4J0U34)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- FENNEL SEED (UNII: G3QC02NIE6)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ZINC PHENOLSULFONATE (UNII: 4O71YT5YB5)
- KOJIC ACID (UNII: 6K23F1TT52)
- LEMON PEEL (UNII: 72O054U628)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Skin Lightening Rodan Fields?
- RxCUI: 1042620 - hydroquinone 2 % Topical Solution
- RxCUI: 1042620 - hydroquinone 20 MG/ML Topical Solution
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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".