Allure Isopropyl Rubbing Alcohol With Wintergreen

Manufacturer: Universal Distribution Center LLC
Effective date: 2024-12-12
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:43:38

Label at a glance#

ProductAllure Isopropyl Rubbing Alcohol With Wintergreen

Active ingredientISOPROPYL ALCOHOL

Label structure12 sections

Indications and uses

to decrease germs in minor cuts and scrapes. helps relieve minor muscular aches due to exertion.

Dosage and administration

clean affected area apply a small amount of this product on the area 1-3 times daily may be covered with a sterile bandage if bandaged, let dry first

Contacts and useful links#

PhoneLabel contact1-800-222-1212

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol (50% conc.)

Purpose

OTC - PURPOSE SECTION

Topical antimicrobial

Uses

INDICATIONS & USAGE SECTION

to decrease germs in minor cuts and scrapes.
helps relieve minor muscular aches due to exertion.

Warnings

WARNINGS SECTION

For external use only

SPL UNCLASSIFIED SECTION

flammable, keep away from fire or flame, heat, spark, electrical.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites or serious burns.

When using this product

OTC - WHEN USING SECTION

do not get into eyes
do not apply over large areas of body
do not use longer than one week unless directed by a doctor

Stop using this product if

OTC - STOP USE SECTION

condition persists or gets worse

Keep this and all drugs out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately

Directions

DOSAGE & ADMINISTRATION SECTION

clean affected area
apply a small amount of this product on the area 1-3 times daily
may be covered with a sterile bandage
if bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

store at room temperature
does not contain, nor is intended as a substitute for grain or ethyl alcohol, will produce serious gastric disturbance if taken internally

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitled

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52000-002-01	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-02	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-03	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-04	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-05	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-06	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-07	2025-07-29	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-01	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-02	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-03	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-04	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-05	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-06	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-07	2020-08-13	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-01	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-02	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-03	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-04	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-05	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-06	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN
52000-002-07	2020-01-31	C162847	48780-1	9d75b9d0-3f34-f424-e053-dadaa90a57ce	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
52000-002-01	Allure Isopropyl Rubbing Alcohol With Wintergreen	118 mL in 1 BOTTLE, PLASTIC	LIQUID	118	3
52000-002-02	Allure Isopropyl Rubbing Alcohol With Wintergreen	177 mL in 1 BOTTLE, PLASTIC	LIQUID	177	3
52000-002-03	Allure Isopropyl Rubbing Alcohol With Wintergreen	237 mL in 1 BOTTLE, PLASTIC	LIQUID	237	3
52000-002-04	Allure Isopropyl Rubbing Alcohol With Wintergreen	296 mL in 1 BOTTLE, PLASTIC	LIQUID	296	3
52000-002-05	Allure Isopropyl Rubbing Alcohol With Wintergreen	355 mL in 1 BOTTLE, PLASTIC	LIQUID	355	3
52000-002-06	Allure Isopropyl Rubbing Alcohol With Wintergreen	414 mL in 1 BOTTLE, PLASTIC	LIQUID	414	3
52000-002-07	Allure Isopropyl Rubbing Alcohol With Wintergreen	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52000-002	ALLURE ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN (ISOPROPYL ALCOHOL) LIQUID [ UNIVERSAL DISTRIBUTION CENTER LLC]	3	Legacy NDC, 7 package rows	20241215_e8899f5a-d251-4d73-8f83-5c8ccfde7848.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	1
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	1
D&C GREEN NO. 5	INACTIVE INGREDIENT	8J6RDU8L9X	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	1
METHYL SALICYLATE	INACTIVE INGREDIENT	LAV5U5022Y	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Allure Isopropyl Rubbing Alcohol With Wintergreen
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52000-002	52000-002-01, 52000-002-02, 52000-002-03, 52000-002-04, 52000-002-05, 52000-002-06, 52000-002-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 45 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, EXTENDED RELEASE / ORAL		3 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	POWDER / ORAL		48 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	GEL / TOPICAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	LOZENGE / ORAL		53 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SOAP / TOPICAL	1.4 %w/w		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	ELIXIR / ORAL	0.3 mg/15ml		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, COATED / ORAL	2.5 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SUSPENSION, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	POWDER, DENTIFRICE / DENTAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	POWDER / TOPICAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SUPPOSITORY / RECTAL	0.11 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SHAMPOO / TOPICAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	PASTE, DENTIFRICE / DENTAL	1.1 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SUSPENSION / ORAL	20 mg/5ml		Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	CAPSULE / ORAL	16 mg		Exact identifier — unii candidate 8 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	GUM, CHEWING / ORAL		2 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	GEL / TOPICAL	0.05 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	GEL / DENTAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	POWDER, FOR SUSPENSION / ORAL		76 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, EXTENDED RELEASE / ORAL		14 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, FILM COATED / ORAL	120 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	SOLUTION / ORAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET / ORAL	80 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	POWDER, FOR SOLUTION / ORAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE / ORAL	20 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SOLUTION / RECTAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	PASTE / DENTAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	TABLET / ORAL	10 mg		Exact identifier — unii candidate 8 equally ranked IID candidates
D&C GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	SOAP / TOPICAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	CAPSULE, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, COATED PELLETS / ORAL	0.01 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SYRUP / ORAL		4 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CONCENTRATE / ORAL	0.03 mg/1ml		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	LOTION / TOPICAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	DOUCHE / VAGINAL	0.05 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
D&C GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	TABLET, COATED / ORAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, LIQUID FILLED / ORAL	1.51 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	GUM, CHEWING / BUCCAL		24 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, DELAYED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET / SUBLINGUAL	0.23 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, CHEWABLE / ORAL		4 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	TABLET / ORAL	0.03 mg		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, DELAYED RELEASE / ORAL	1.9 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C YELLOW NO. 10	D&C YELLOW NO. 10	35SW5USQ3G	SOLUTION / ORAL		8 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	SHAMPOO / TOPICAL	0.09 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
246bc69c-a906-4ef6-9204-0451114ef876			e8899f5a-d251-4d73-8f83-5c8ccfde7848	2024-12-12	Warnings	Exact identifier spl id: 246bc69c-a906-4ef6-9204-0451114ef876 spl set id: e8899f5a-d251-4d73-8f83-5c8ccfde7848

Reported adverse events (FAERS/openFDA)#

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