NDC 30142-111 Oral Saline Laxative Ginger Lemon
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 30142 - The Kroger Company
- 30142-111 - Oral Saline Laxative
Product Packages
NDC Code 30142-111-12
Package Description: 1 BOTTLE in 1 CARTON / 45 mL in 1 BOTTLE
Product Details
What is NDC 30142-111?
What are the uses for Oral Saline Laxative Ginger Lemon?
Which are Oral Saline Laxative Ginger Lemon UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
Which are Oral Saline Laxative Ginger Lemon 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Oral Saline Laxative Ginger Lemon?
- RxCUI: 282725 - sodium phosphate, dibasic 2.7 GM / sodium phosphate, monobasic 7.2 GM in 15 mL Oral Solution
- RxCUI: 282725 - sodium phosphate, dibasic 180 MG/ML / sodium phosphate, monobasic 480 MG/ML Oral Solution
- RxCUI: 282725 - sodium phosphate, dibasic 2.7 GM / sodium phosphate, monobasic 7.2 GM per 15 ML Oral Solution
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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".