NDC 58443-0327 Australian Gold Aloe Gel With Lidocaine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises, Inc.
- 58443-0327 - Australian Gold
Product Characteristics
Product Packages
NDC Code 58443-0327-4
Package Description: 237 mL in 1 BOTTLE
Product Details
What is NDC 58443-0327?
What are the uses for Australian Gold Aloe Gel With Lidocaine?
Which are Australian Gold Aloe Gel With Lidocaine UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Australian Gold Aloe Gel With Lidocaine 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:
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALLANTOIN (UNII: 344S277G0Z)
- SCOTCH SPEARMINT OIL (UNII: I5T0098W81)
- PEG-60 LANOLIN (UNII: K2OI1D27ET)
- CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
- BEE POLLEN (UNII: 3729L8MA2C)
- COMFREY LEAF (UNII: DG4F8T839X)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- ALPHA-TOCOPHERYLQUINONE (UNII: ZO763K43XR)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER 1342 (UNII: 809Y72KV36)
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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".