Glover's Anti-Dandruff Ointment

Manufacturer: J. Strickland & Co.
Effective date: 2023-10-21
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:58:31

Label at a glance#

ProductGlovers Anti-Dandruff

Active ingredientSULFUR, SALICYLIC ACID

Label structure7 sections

Indications and uses

relieves the itching and scaling associated with dandruff

Dosage and administration

Apply a small amount to the scalp one to four times daily or as directed by a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Sulfur, 5%

Salicylic Acid, 3%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Uses

INDICATIONS & USAGE SECTION

relieves the itching and scaling associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Do not get in eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and consult a doctor if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount to the scalp one to four times daily or as directed by a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petrolatum, Mineral Oil, Glyceryl Tribehenate, Arachidyl Propionate, Fragrance, Polysorbate-20, Propylparaben, Iron Oxides, Talc.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-009-00

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-009-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247682	salicylic acid 3 % / sulfur 5 % Topical Ointment	PSN	3
247682	salicylic acid 0.03 MG/MG / sulfur 0.05 MG/MG Topical Ointment	SCD	3
247682	salicylic acid 3 % / sulfur 5 % Topical Ointment	SY	3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
12022-009-00	Glovers Anti-Dandruff	28 g in 1 JAR	OINTMENT	28		3
12022-009-01	Glovers Anti-Dandruff	99 g in 1 JAR	OINTMENT	99		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
12022-009	GLOVERS ANTI-DANDRUFF (SULFUR, SALICYLIC ACID) OINTMENT [J. STRICKLAND & CO.]	3	Current NDC, Legacy NDC, 2 package rows	20231101_49fd4e03-736c-429a-8972-7302b732f816.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Glovers Anti-Dandruff
Sulfur, Salicylic Acid
PETROLATUM
MINERAL OIL
TRIBEHENIN
ARACHIDYL PROPIONATE
POLYSORBATE 20
PROPYLPARABEN
FERRIC OXIDE RED
TALC
SULFUR
SALICYLIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
12022-009	12022-009-00, 12022-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PETROLATUM	4T6H12BN9U	IACT
MINERAL OIL	T5L8T28FGP	IACT
TRIBEHENIN	8OC9U7TQZ0	IACT
ARACHIDYL PROPIONATE	QV5DAH3MSB	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
PROPYLPARABEN	Z8IX2SC1OH	IACT
FERRIC OXIDE RED	1K09F3G675	IACT
TALC	7SEV7J4R1U	IACT
SULFUR	70FD1KFU70	ACTIB
SALICYLIC ACID	O414PZ4LPZ	ACTIB

Source Document#

Source XML

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
Glovers Anti-Dandruff	SULFUR, SALICYLIC ACID	J. Strickland & Co.	49fd4e03-736c-429a-8972-7302b732f816	2023-10-21	Warnings	Exact identifier ndc (package): 12022-009-01 ndc (package): 12022-009-00 ndc (product): 12022-009 ndc11 (package): 12022000900 ndc11 (package): 12022000901 spl id: 083342a6-c300-f132-e063-6294a90a502e spl set id: 49fd4e03-736c-429a-8972-7302b732f816

Reported adverse events (FAERS/openFDA)#

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