NDC 76849-201 4rlf Topical Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76849 - Rinati Skin, Llc
- 76849-201 - 4rlf Topical Analgesic
Product Packages
NDC Code 76849-201-11
Package Description: 1 BLISTER PACK in 1 CARTON / 10 VIAL in 1 BLISTER PACK / 1 mL in 1 VIAL
Product Details
What is NDC 76849-201?
What are the uses for 4rlf Topical Analgesic?
Which are 4rlf Topical Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are 4rlf Topical Analgesic 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)
- OCIMUM TENUIFLORUM WHOLE (UNII: 7OS52KZ33J)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- WATER (UNII: 059QF0KO0R)
- WITHANIA SOMNIFERA ROOT (UNII: V038D626IF)
- PIPER NIGRUM WHOLE (UNII: 49L10LI8DN)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
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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".