NDC 73622-3077 Hemorrhoidal Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73622 - Curetech Skincare
- 73622-3077 - Hemorrhoidal Relief Cream
Product Packages
NDC Code 73622-3077-5
Package Description: 28.3 g in 1 TUBE
Product Details
What is NDC 73622-3077?
What are the uses for Hemorrhoidal Relief Cream?
Which are Hemorrhoidal Relief Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Hemorrhoidal Relief Cream 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- CHAMOMILE (UNII: FGL3685T2X)
- CHLOROCRESOL (UNII: 36W53O7109)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CORN OIL (UNII: 8470G57WFM)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- COCONUT OIL (UNII: Q9L0O73W7L)
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- TRICAPRILIN (UNII: 6P92858988)
- MENTHOL (UNII: L7T10EIP3A)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
What is the NDC to RxNorm Crosswalk for Hemorrhoidal Relief Cream?
- RxCUI: 2529640 - lidocaine 4 % / phenylephrine hydrochloride 0.25 % Rectal Cream
- RxCUI: 2529640 - lidocaine 40 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Rectal 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".