NDC 51830-054 Preparing Tonic
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51830-054?
What are the uses for Preparing Tonic?
Which are Preparing Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Preparing Tonic 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:
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALLANTOIN (UNII: 344S277G0Z)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- IMIDUREA (UNII: M629807ATL)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- ALCOHOL (UNII: 3K9958V90M)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
What is the NDC to RxNorm Crosswalk for Preparing Tonic?
- RxCUI: 245199 - salicylic acid 1 % Topical Lotion
- RxCUI: 245199 - salicylic acid 10 MG/ML Topical Lotion
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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".