NDC 33346-3400 Relief Recovery
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33346 - Mayway Corporation
- 33346-3400 - Relief Recovery
Product Packages
NDC Code 33346-3400-1
Package Description: 1 VIAL, GLASS in 1 BOX / 50 mL in 1 VIAL, GLASS (33346-3400-2)
Product Details
What is NDC 33346-3400?
What are the uses for Relief Recovery?
Which are Relief Recovery UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- CAMPHOR OIL (UNII: 75IZZ8Y727) (Active Moiety)
- CAPSICUM OLEORESIN (UNII: UW86K581WY)
- CAPSICUM OLEORESIN (UNII: UW86K581WY) (Active Moiety)
Which are Relief Recovery 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:
- BORNEOL (UNII: M89NIB437X)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
- CARTHAMUS TINCTORIUS FLOWER OIL (UNII: SDQ136WIM5)
- ANGELICA PUBESCENS WHOLE (UNII: SV5CN7O3MB)
- LIGUSTICUM SINENSE SUBSP. CHUANXIONG WHOLE (UNII: CAX256379F)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
- MYRRH OIL (UNII: H74221J5J4)
- ARNEBIA EUCHROMA ROOT (UNII: F6W6210OKY)
- MINERAL OIL (UNII: T5L8T28FGP)
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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".