NDC 72136-004 Recovery Balm - Ultra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329)
Code Structure Chart
Product Details
What is NDC 72136-004?
What are the uses for Recovery Balm - Ultra?
Which are Recovery Balm - Ultra UNII Codes?
The UNII codes for the active ingredients in this product are:
- MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
Which are Recovery Balm - Ultra 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SQUALENE (UNII: 7QWM220FJH)
- PERSIC OIL (UNII: 5M26W7T072)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- SESAME OIL (UNII: QX10HYY4QV)
- JOJOBA OIL (UNII: 724GKU717M)
- ALLANTOIN (UNII: 344S277G0Z)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- MAGNESIUM CHLORIDE TETRAHYDRATE (UNII: H2K2KVE749)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- DIPTERYX ODORATA SEED (UNII: D43A5L1U6L)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SWEET MARJORAM OIL (UNII: ICH7BE016E)
- HELICHRYSUM ARENARIUM FLOWER (UNII: GN27F71368)
- CANANGA OIL (UNII: 8YOY78GNNX)
- TANACETUM VULGARE FLOWER (UNII: 392XZ1456Q)
- LAPONITE (UNII: D703131383)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
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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".