Isopropyl Alcohol with Wintergreen 70%

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: Isopropyl Alcohol with Wintergreen 70%
Generic name: ISOPROPYL ALCOHOL WITH WINTERGREEN 70%
Manufacturer: Hydrox Laboratories
Product type: HUMAN OTC DRUG
SPL set ID: 5845f723-8866-4738-bec6-621041899f57
SPL ID: 48337b0f-9b82-7607-e063-6394a90a1d15
Version: 11
Effective date: 2026-01-12
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 06:05:56

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Isopropyl Alcohol with Wintergreen 70%	openfda.brand_name
generic name		ISOPROPYL ALCOHOL WITH WINTERGREEN 70%	openfda.generic_name
manufacturer name		Hydrox Laboratories	openfda.manufacturer_name
ndc	package	10565-006-16	openfda.package_ndc
ndc	package	10565-006-08	openfda.package_ndc
ndc	package	10565-006-04	openfda.package_ndc
ndc	package	10565-006-99	openfda.package_ndc
ndc	package	10565-006-32	openfda.package_ndc
ndc	product	10565-006	openfda.product_ndc
ndc11	package	10565000632	derived:openfda.package_ndc
ndc11	package	10565000699	derived:openfda.package_ndc
ndc11	package	10565000616	derived:openfda.package_ndc
ndc11	package	10565000608	derived:openfda.package_ndc
ndc11	package	10565000604	derived:openfda.package_ndc
rxcui		808520	openfda.rxcui
spl id		48337b0f-9b82-7607-e063-6394a90a1d15	id
spl set id		5845f723-8866-4738-bec6-621041899f57	set_id
unii		ND2M416302	openfda.unii

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only Flammable Keep away from fire or flame, heat, spark, electrical. Flash point 72°F. do not use with eletocautery procedures. Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns. When using this product do not get into eyes do not apply over large areas of the body do not use longer than 1 week unless directed by a doctor Stop use and ask a doctor if condition persists or gets worse

warnings and cautions

Other information does not contain, nor is intended as a substitue for grain or ethyl alcohol. will produce serious gastric disturbances if taken internally.

Reported adverse events (FAERS/openFDA)#

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