NDC 63788-111 Lid O Creme Roll On
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63788 - Pharma Natural, Inc.
- 63788-111 - Lid O Creme Roll On
Product Packages
NDC Code 63788-111-25
Package Description: 71 g in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 63788-111?
What are the uses for Lid O Creme Roll On?
Which are Lid O Creme Roll On UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Lid O Creme Roll On 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- ALMOND OIL (UNII: 66YXD4DKO9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
What is the NDC to RxNorm Crosswalk for Lid O Creme Roll On?
- RxCUI: 1595624 - lidocaine HCl 4 % / menthol 1 % Topical Cream
- RxCUI: 1595624 - lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML Topical Cream
- RxCUI: 1595624 - lidocaine hydrochloride 4 % / menthol 1 % Topical Cream
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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".