Cold Armor

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: Cold Armor
Generic name: ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM
Manufacturer: Ratis, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 46af3f19-055e-4025-a14e-1d6c25880f4d
SPL ID: fb97f830-fce0-4a6d-81cf-ae5d2abe5de7
Version: 1
Effective date: 2023-05-26
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:27

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Cold Armor	openfda.brand_name
generic name		ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM	openfda.generic_name
manufacturer name		Ratis, LLC	openfda.manufacturer_name
ndc	package	71753-1156-1	openfda.package_ndc
ndc	product	71753-1156	openfda.product_ndc
ndc11	package	71753115601	derived:openfda.package_ndc
spl id		fb97f830-fce0-4a6d-81cf-ae5d2abe5de7	id
spl set id		46af3f19-055e-4025-a14e-1d6c25880f4d	set_id
unii		269XH13919	openfda.unii
unii		KPS1B1162N	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		492225Q21H	openfda.unii
unii		8E272251DI	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		T4423S18FM	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

WARNINGS: Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician. Stop use and ask a doctor if symptoms persist for more than 2 days. For oral use only. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control center right away. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING

Reported adverse events (FAERS/openFDA)#

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