NDC 68093-7151 Stingeze Max Insect Bite Relief
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68093-7151?
What are the uses for Stingeze Max Insect Bite Relief?
Which are Stingeze Max Insect Bite Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Stingeze Max Insect Bite Relief 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Stingeze Max Insect Bite Relief?
- RxCUI: 1485210 - benzocaine 10 % / camphor 3 % / phenol 1.35 % Topical Solution
- RxCUI: 1485210 - benzocaine 100 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution
- RxCUI: 1485215 - StingEze MAX 10 % / 3 % / 1.35 % Topical Solution
- RxCUI: 1485215 - benzocaine 100 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution [Stingeze Max]
- RxCUI: 1485215 - Stingeze Max (benzocaine 10 % / camphor 3 % / phenol 1.35 % ) 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".