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 01:50:24

Label at a glance#

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type
1246528	hydrocortisone 25 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream	hydrocortisone 25 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream	SCD Active
1294025	Hydrocortisone/Pramoxine (Rectal)	hydrocortisone acetate 25 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream	SCD Active
1234506	Hydrocortisone/Pramoxine (Topical)	hydrocortisone acetate 25 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream	SCD Active

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
45802-472-53	GM - Gram	45802-472	56b71bf4-5df3-4cec-be2c-70a8db887f4c	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
45802-472	45802-472-53

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
Hydrocortisone Acetate Pramoxine Hcl	HYDROCORTISONE ACETATE PRAMOXINE HCL	Padagis Israel Pharmaceuticals Ltd	87a4c494-56f9-48f6-8592-d610c507a4fc	2022-05-31	Adverse reactions	Exact identifier ndc (package): 45802-472-53 ndc11 (package): 45802047253

Reported adverse events (FAERS/openFDA)#

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