NDC 49631-182 Ohtas Isan Antacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49631 - Ohta's Isan Co., Ltd
- 49631-182 - Ohtas Isan Antacid
Product Characteristics
Product Packages
NDC Code 49631-182-11
Package Description: 1 PACKAGE in 1 CARTON / 40 TABLET in 1 PACKAGE
Product Details
What is NDC 49631-182?
What are the uses for Ohtas Isan Antacid?
Which are Ohtas Isan Antacid UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALMASILATE (UNII: OZQ8O62H53)
- ALMASILATE (UNII: OZQ8O62H53) (Active Moiety)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- BICARBONATE ION (UNII: HN1ZRA3Q20) (Active Moiety)
Which are Ohtas Isan Antacid 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:
- CINNAMON (UNII: 5S29HWU6QB)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- TANGERINE (UNII: KH3E3096OO)
- CLOVE (UNII: K48IKT5321)
- CLOVE OIL (UNII: 578389D6D0)
- FENNEL (UNII: 557II4LLC3)
- FENNEL OIL (UNII: 59AAO5F6HT)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- LEMON OIL (UNII: I9GRO824LL)
- MENTHOL (UNII: L7T10EIP3A)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- NUTMEG (UNII: AEE24M3MQ9)
- PICRASMA QUASSIOIDES WOOD (UNII: 75EIV4LX7W)
What is the NDC to RxNorm Crosswalk for Ohtas Isan Antacid?
- RxCUI: 1363382 - almasilate 125 MG / calcium carbonate 200 MG / sodium bicarbonate 200 MG Chewable Tablet
- RxCUI: 1363382 - aluminum magnesium silicate 125 MG / calcium carbonate 200 MG / sodium bicarbonate 200 MG Chewable Tablet
- RxCUI: 1363382 - aluminum magnesium silicate 125 MG / Calcium Carbonate 200 MG / NaHCO3 200 MG Chewable Tablet
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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".