NDC 77338-410 Hemorrhoidalcreampro
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77338 - Astonea Labs Private Limited
- 77338-410 - Hemorrhoidalcreampro
Product Packages
NDC Code 77338-410-55
Package Description: 56.6 g in 1 TUBE
Product Details
What is NDC 77338-410?
What are the uses for Hemorrhoidalcreampro?
Which are Hemorrhoidalcreampro UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINERAL OIL (UNII: T5L8T28FGP)
- MINERAL OIL (UNII: T5L8T28FGP) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Hemorrhoidalcreampro 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)
- WHITE WAX (UNII: 7G1J5DA97F)
- THYMUS VULGARIS LEAF (UNII: GRX3499643)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- CORN OIL (UNII: 8470G57WFM)
- GLYCERIN (UNII: PDC6A3C0OX)
- LANOLIN (UNII: 7EV65EAW6H)
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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".