DALEKTRO N

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: DALEKTRO N
Generic name: SILVER NITRATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, COBALTOUS NITRATE HEXAHYDRATE, CUPRIC ACETATE, IRON, POTASSIUM CARBONATE, MAGNESIUM CHLORIDE, MANGANESE ACETATE TETRAHYDRATE, SELENIUM, SILICON DIOXIDE, AND ZINC PHOSPHIDE
Manufacturer: PEKANA Natruheilmittel GmbH
Product type: HUMAN OTC DRUG
SPL set ID: 2b39ce30-54ff-4586-bda1-d9410140b26e
SPL ID: 7ee0a73a-1bb7-4e4e-80b2-d1ef6920c069
Version: 2
Effective date: 2023-01-11
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:30

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		DALEKTRO N	openfda.brand_name
generic name		SILVER NITRATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, COBALTOUS NITRATE HEXAHYDRATE, CUPRIC ACETATE, IRON, POTASSIUM CARBONATE, MAGNESIUM CHLORIDE, MANGANESE ACETATE TETRAHYDRATE, SELENIUM, SILICON DIOXIDE, AND ZINC PHOSPHIDE	openfda.generic_name
manufacturer name		PEKANA Natruheilmittel GmbH	openfda.manufacturer_name
ndc	package	59469-305-10	openfda.package_ndc
ndc	package	59469-305-40	openfda.package_ndc
ndc	product	59469-305	openfda.product_ndc
ndc11	package	59469030510	derived:openfda.package_ndc
ndc11	package	59469030540	derived:openfda.package_ndc
spl id		7ee0a73a-1bb7-4e4e-80b2-d1ef6920c069	id
spl set id		2b39ce30-54ff-4586-bda1-d9410140b26e	set_id
unii		02F3473H9O	openfda.unii
unii		813396S1PC	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		9TO51D176N	openfda.unii
unii		2E32821G6I	openfda.unii
unii		39M11XPH03	openfda.unii
unii		2H2166872F	openfda.unii
unii		E1UOL152H7	openfda.unii
unii		H6241UJ22B	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat.

Reported adverse events (FAERS/openFDA)#

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