National Council for Prescription Drug Programs indexing - billing unit

Manufacturer: National Council for Prescription Drug Programs
Effective date: 2012-07-24
Label type: Indexing - Billing Unit
Version: 1
Source: full-release
Hydrated at: 2026-06-05 03:10:42

Label at a glance#

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1313925	Alpha tocopherol/Ascorbic acid/Beta carotene/Calcium carbonate/Cholecalciferol/Docusate/Ferrous fumarate/Folic acid/Niacinamide/Pantothenate/Pyridoxine/Riboflavin/Thiamine/Vitamin B12/Zinc oxide (Oral Pill)	alpha-tocopherol acetate 30 UNT / ascorbic acid 100 MG / beta carotene 1000 UNT / calcium carbonate 200 MG / calcium pantothenate 7 MG / cholecalciferol 400 UNT / docusate sodium 25 MG / ferrous fumarate 29 MG / folic acid 1 MG / niacinamide 15 MG / pyridoxine hydrochloride 20 MG / riboflavin 3 MG / thiamine 3 MG / vitamin B12 0.012 MG / zinc oxide 20 MG Oral Tablet	SCD Active

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
13925-116-01	EA - Each	13925-116	f8a80b30-6ccc-4641-be3f-55847f3289bc	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
13925-116	13925-116-01

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Se-Natal 19	.BETA.-CAROTENE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM PANTOTHENATE, CALCIUM CARBONATE, FERROUS FUMARATE, ZINC OXIDE AND DOCUSATE SODIUM	Seton Pharmaceuticals	635104e6-6a53-4684-ac9a-7ac31b33083d	2025-02-24	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 13925-116-01 ndc11 (package): 13925011601

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.