NDC 21130-143 Signature Care Bite And Sting Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21130 - Safeway
- 21130-143 - Signature Care Bite And Sting Relief
Product Packages
NDC Code 21130-143-01
Package Description: 85 g in 1 CAN
Product Details
What is NDC 21130-143?
What are the uses for Signature Care Bite And Sting Relief?
Which are Signature Care Bite And Sting Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Signature Care Bite And Sting 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CLOVE OIL (UNII: 578389D6D0)
- PEPPERMINT (UNII: V95R5KMY2B)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CORN OIL (UNII: 8470G57WFM)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- ALCOHOL (UNII: 3K9958V90M)
- CHAMOMILE (UNII: FGL3685T2X)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
What is the NDC to RxNorm Crosswalk for Signature Care Bite And Sting Relief?
- RxCUI: 238909 - benzocaine 5 % Topical Spray
- RxCUI: 238909 - benzocaine 50 MG/ML Topical Spray
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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".