Caffeine and Sodium Benzoate

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Caffeine and Sodium Benzoate
Generic name: CAFFEINE AND SODIUM BENZOATE
Manufacturer: American Regent, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: b2c6b352-f837-4903-8e4c-fb0a2b20bb60
SPL ID: 53245845-b446-46f8-bbe8-3323c58e10e5
Version: 7
Effective date: 2019-12-06
Source export date: 2026-10-12
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:05:21

Harmonized routes table
Harmonized routes
INTRAMUSCULAR, INTRAVENOUS

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Caffeine and Sodium Benzoate	openfda.brand_name
generic name		CAFFEINE AND SODIUM BENZOATE	openfda.generic_name
manufacturer name		American Regent, Inc.	openfda.manufacturer_name
ndc	package	0517-2502-01	openfda.package_ndc
ndc	package	0517-2502-10	openfda.package_ndc
ndc	product	0517-2502	openfda.product_ndc
ndc11	package	00517250201	derived:openfda.package_ndc
ndc11	package	00517250210	derived:openfda.package_ndc
spl id		53245845-b446-46f8-bbe8-3323c58e10e5	id
spl set id		b2c6b352-f837-4903-8e4c-fb0a2b20bb60	set_id
unii		3G6A5W338E	openfda.unii

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