NDC 51514-0327 Yes To Tomatoes Roller Ball Spot Stick
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51514 - Autumn Harp, Inc.
- 51514-0327 - Yes To Tomatoes Roller Ball Spot Stick
Product Packages
NDC Code 51514-0327-1
Package Description: 14.7 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 51514-0327?
What are the uses for Yes To Tomatoes Roller Ball Spot Stick?
Which are Yes To Tomatoes Roller Ball Spot Stick 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 Yes To Tomatoes Roller Ball Spot Stick 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)
- ALCOHOL (UNII: 3K9958V90M)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- PROPANEDIOL (UNII: 5965N8W85T)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- GRAPEFRUIT JUICE (UNII: JQ9EK2H6BG)
- PHENETHYL ALCOHOL (UNII: ML9LGA7468)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POMEGRANATE JUICE (UNII: 99S671U9KB)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- LEVOMENOL (UNII: 24WE03BX2T)
- TEA TREE OIL (UNII: VIF565UC2G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TOMATO (UNII: Z4KHF2C175)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GINGER (UNII: C5529G5JPQ)
- LIMONENE, (+/-)- (UNII: 9MC3I34447)
What is the NDC to RxNorm Crosswalk for Yes To Tomatoes Roller Ball Spot Stick?
- RxCUI: 251577 - salicylic acid 2 % Topical Solution
- RxCUI: 251577 - salicylic acid 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".