maxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen

Manufacturer: OSTL, INC. | WILSON MEDICINE COMPANY
Effective date: 2018-07-27
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:56:28

Label at a glance#

Productmaxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen

Active ingredientISOPROPYL ALCOHOL

Label structure10 sections

Indications and uses

helps prevent the risk of infection in:• minor cuts • scrapes • burns

Dosage and administration

• Clean affected area • spray a small amount of this product on the area 1 to 3 times daily • may be covered with sterile bandage • if bandaged, let dry first

Storage and handling

• Keep tightly closed and at controlled room temperature • does not contain, nor is intended as a substitute for grain or ethyl alcohol • will produce serious gastric disturbances if taken internally

Contacts and useful links#

PhonePoison Help1-800-222-1222

Websitewww.ostltrade.com

WWW.OSTLTRADE.COM

Label contents#

Full prescribing information#

Active ingredients (by volume)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol (50%Conc)

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

helps prevent the risk of infection in:• minor cuts • scrapes • burns

Warnings

WARNINGS SECTION

For external use only

Flammable • keep away from fire or flame, heat, spark, electrical

Ask a doctor before use for deep or puncture wounds, animal bites or serious burns

When using this products • do not get in to eyes • do not inhale • do not apply over large areas of the body • do not use longer than 1 week

Stop use and ask a doctor if condition persists or gets worse

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. if swallowed, get medical help or contact poison control center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean affected area • spray a small amount of this product on the area 1 to 3 times daily • may be covered with sterile bandage • if bandaged, let dry first

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified water, methyl salicylate, D&C Green #5, D&C Yellow #10

Other information

STORAGE AND HANDLING SECTION

SPL UNCLASSIFIED SECTION

FIRST AID ANTISEPTIC

For Rubbing & Massaging

Caution: Do not point at self or others, product will squirt when squeezed. Use only in a well-ventilated area; fumes can be harmful.

Made in India

Imported by : OSTL Inc.

5805 White Oak Ave Encino CA, 91416

WWW.OSTLTRADE.COM

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

355 mL

295 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616456	isopropyl alcohol 50 % Topical Solution	PSN	3
616456	isopropyl alcohol 0.5 ML/ML Topical Solution	SCD	3
616456	isopropyl alcohol 50 % Topical Solution	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69950-004-01	2023-01-30	C162847	48780-1	f386c64a-4260-0266-e053-dadaa90a7c1a	maxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen
69950-004-02	2023-01-30	C162847	48780-1	f386c64a-4260-0266-e053-dadaa90a7c1a	maxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69950-004-01	maxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen	355 mL in 1 BOTTLE, PLASTIC	LIQUID	355		3
69950-004-02	maxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen	295 mL in 1 BOTTLE, PLASTIC	LIQUID	295		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69950-004	MAXIM 50% ISOPROPYL RUBBING ALCOHOL WITH WINTERGREEN (ISOPROPYL ALCOHOL) LIQUID [OSTL, INC.]	3	Legacy NDC, 2 package rows	20180730_5490b947-61f4-434e-9939-563c4a2ddbd5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	2
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	2
D&C GREEN NO. 5	INACTIVE INGREDIENT	8J6RDU8L9X	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	2
METHYL SALICYLATE	INACTIVE INGREDIENT	LAV5U5022Y	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

maxim 50% ISOPROPYL RUBBING ALCOHOL With Wintergreen
ISOPROPYL ALCOHOL
WATER
METHYL SALICYLATE
D&C GREEN NO. 5
D&C YELLOW NO. 10

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69950-004	69950-004-01, 69950-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT
METHYL SALICYLATE	LAV5U5022Y	IACT
D&C GREEN NO. 5	8J6RDU8L9X	IACT
D&C YELLOW NO. 10	35SW5USQ3G	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
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	DOUCHE / VAGINAL	0.05 %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	PASTE, DENTIFRICE / DENTAL	1.1 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	TABLET / ORAL	10 mg		Exact identifier — unii candidate 8 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	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	SOLUTION / ORAL		8 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, CHEWABLE / ORAL		4 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
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 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 / ORAL	20 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	PASTE / DENTAL	NA		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 GREEN NO. 5	D&C GREEN NO. 5	8J6RDU8L9X	SOAP / TOPICAL	NA		Exact identifier — unii candidate 6 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	CAPSULE, LIQUID FILLED / ORAL	1.51 mg		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	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	SUSPENSION, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 31 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
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
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	POWDER, DENTIFRICE / DENTAL	NA		Exact identifier — unii candidate 8 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
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	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	TABLET / ORAL	80 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 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	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	CAPSULE, COATED PELLETS / ORAL	0.01 mg		Exact identifier — unii candidate 31 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	TABLET, EXTENDED RELEASE / ORAL		14 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
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, DELAYED RELEASE / ORAL	1.9 mg		Exact identifier — unii candidate 31 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	SHAMPOO / TOPICAL	NA		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
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
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	SUPPOSITORY / RECTAL	0.11 mg		Exact identifier — unii candidate 31 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
9924e1d6-a301-4f8a-999c-c17d23b7fe2b			5490b947-61f4-434e-9939-563c4a2ddbd5	2018-07-27	Warnings	Exact identifier spl id: 9924e1d6-a301-4f8a-999c-c17d23b7fe2b spl set id: 5490b947-61f4-434e-9939-563c4a2ddbd5

Reported adverse events (FAERS/openFDA)#

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