NDC 15370-102 Quflora Fe Pediatric Drops
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 15370 - Carwin Pharmaceutical Associates, Llc
- 15370-102 - Quflora Fe Pediatric Drops
Product Characteristics
Product Packages
NDC Code 15370-102-50
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 50 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 15370-102?
What are the uses for Quflora Fe Pediatric Drops?
Which are Quflora Fe Pediatric Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
- RETINOL (UNII: G2SH0XKK91) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9) (Active Moiety)
- THIAMINE HYDROCHLORIDE (UNII: M572600E5P)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
- LEVOMEFOLATE GLUCOSAMINE (UNII: Q65PL71Q1A)
- LEVOMEFOLATE GLUCOSAMINE (UNII: Q65PL71Q1A) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- FERROUS SULFATE (UNII: 39R4TAN1VT)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Quflora Fe Pediatric Drops 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:
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- PROPYLENE (UNII: AUG1H506LY)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
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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".