FDA label 8ac90f3f-d838-4da8-b1ac-38ab1af2e2dd

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)

SPL set ID: 1f72fdc4-7dfa-40e6-bd84-de78f5cbd569
SPL ID: 8ac90f3f-d838-4da8-b1ac-38ab1af2e2dd
Version: 2
Effective date: 2017-08-01
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 03:02:30

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		8ac90f3f-d838-4da8-b1ac-38ab1af2e2dd	id
spl set id		1f72fdc4-7dfa-40e6-bd84-de78f5cbd569	set_id

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 For oral use only. When using this product Avoid contact with eyes. In case of accidental contact with eyes, flush with water and immediately seek professional help. Stop use and ask a doctor if symptoms persist or are accompanied by fever. Zicam ® Cold Remedy Plus was formulated to shorten the duration of the common cold and was not formulated to be effective for flu or allergies. If you are allergic or sensitive to zinc, consult a doctor before using. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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