NDC 71629-035 Willow Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 71629-035?
What are the uses for Willow Balm?
Which are Willow Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Willow Balm 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:
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- HELICHRYSUM GYMNOCEPHALUM WHOLE (UNII: 0369G6I64W)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ALMOND OIL (UNII: 66YXD4DKO9)
- TROLAMINE (UNII: 9O3K93S3TK)
- CETEARETH-10 (UNII: K9YLE2L8PA)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SPEARMINT (UNII: J7I2T6IV1N)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N)
- .ALPHA.,.ALPHA.-DIBROMO-D-CAMPHOR (UNII: F89Z8SAG3O)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Willow Balm?
- RxCUI: 1442261 - menthol 3 % Topical Cream
- RxCUI: 1442261 - menthol 30 MG/ML Topical Cream
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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".