ActivICE

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: ActivICE
Generic name: MENTHOL
Manufacturer: Medline Industries, LP
Product type: HUMAN OTC DRUG
SPL set ID: 834adeb9-38ad-0cfe-e053-2991aa0af82f
SPL ID: 5a6e9886-23df-e0ee-e063-6294a90a5e48
Version: 12
Effective date: 2026-09-01
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:54

Harmonized routes table
Harmonized routes
TOPICAL

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		ActivICE	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Medline Industries, LP	openfda.manufacturer_name
ndc	package	53329-984-06	openfda.package_ndc
ndc	package	53329-984-30	openfda.package_ndc
ndc	package	53329-984-04	openfda.package_ndc
ndc	package	53329-984-23	openfda.package_ndc
ndc	package	53329-984-25	openfda.package_ndc
ndc	package	53329-984-16	openfda.package_ndc
ndc	product	53329-984	openfda.product_ndc
ndc11	package	53329098423	derived:openfda.package_ndc
ndc11	package	53329098404	derived:openfda.package_ndc
ndc11	package	53329098406	derived:openfda.package_ndc
ndc11	package	53329098425	derived:openfda.package_ndc
ndc11	package	53329098416	derived:openfda.package_ndc
ndc11	package	53329098430	derived:openfda.package_ndc
rxcui		2119857	openfda.rxcui
rxcui		283257	openfda.rxcui
spl id		5a6e9886-23df-e0ee-e063-6294a90a5e48	id
spl set id		834adeb9-38ad-0cfe-e053-2991aa0af82f	set_id
unii		L7T10EIP3A	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 For external use only. Avoid contact with eyes. Flammable: keep away from fire or flame. When using this product use only as directed do not bandage tightly or use with heating pad do not apply to wounds or damaged skin Stop use and ask doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days redness is present excessive irritation of the skin develops If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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