FDA.reportPublic FDA data

Neutrogena T/Gel Therapeutic Extra Strength

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2023-03-14
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:33:15

Label at a glance#

ProductNeutrogena T/Gel Therapeutic Extra Strength
Active ingredientCOAL TAR
Label structure11 sections

Dosage and administration

For best results, use at least twice a week or as directed by a doctor. Wet hair thoroughly. Massage shampoo into your scalp. Lather, leaving on your hair and scalp for several minutes. Rinse and repeat.

Storage and handling

In rare instances, temporary discoloration of gray, blonde, bleached, or tinted hair may occur. Store away from direct sunlight. Store at room temperature.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Coal Tar 1%
(4% Neutar ® Solubilized Coal Tar Extract)

Purpose

OTC - PURPOSE SECTION

Anti-dandruff, Anti-seborrheic dermatitis, Anti-psoriasis

Use

INDICATIONS & USAGE SECTION

Controls the symptoms of dandruff, seborrheic dermatitis and psoriasis.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • for prolonged periods without consulting a doctor.
  • this product with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs unless directed to do so by a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have a condition that covers a large area of the body.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
  • Use caution when exposing skin to sunlight after applying this product. It may increase your tendency to sunburn for up to 24 hours after application.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

* WARNING: This product contains chemicals known to the State of California to cause cancer.

Directions

DOSAGE & ADMINISTRATION SECTION

For best results, use at least twice a week or as directed by a doctor.

  • Wet hair thoroughly.
  • Massage shampoo into your scalp.
  • Lather, leaving on your hair and scalp for several minutes.
  • Rinse and repeat.

Other information

STORAGE AND HANDLING SECTION

In rare instances, temporary discoloration of gray, blonde, bleached, or tinted hair may occur. Store away from direct sunlight. Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Polysorbate-20, Laureth-4, Cocamidopropyl Betaine, Cocamide MEA, Fragrance, PEG-120 Methyl Glucose Dioleate, Sodium Chloride, Bis-hydroxyethyl Dihydroxypropyl Stearammonium Chloride, DMDM Hydantoin, Citric Acid, Tetrasodium EDTA, Sodium Hydroxide, Triethanolamine

Questions?

OTC - QUESTIONS SECTION

Call toll-free 877-256-4247 or 215-273-8755 (collect). www.neutrogena.com

SPL UNCLASSIFIED SECTION

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 177 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEUTROGENA ®

T/GEL ®

therapeutic

shampoo

Extra Strength

controls redness,

intense itching and

flaking of severe

scalp conditions

  • Starts working after

    just one use
  • dandruff, psoriasis,

    seborrheic dermatitis

DERMATOLOGIST

RECOMMENDED BRAND

Neutrogena ®

4% NEUTAR ®

(Coal tar 1.0%)

6 FL OZ (177 mL)

Ntg001Ntg001

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69968-0694-6ML - Milliliter69968-069402559e6c-1a4e-4d12-a3ef-d905edac6a9f12022-06-06

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-069469968-0694-6, 69968-0694-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
POLYSORBATE 207T1F30V5YHIACT
LAURETH-46HQ855798JIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCO MONOETHANOLAMIDEC80684146DIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
SODIUM CHLORIDE451W47IQ8XIACT
BIS-HYDROXYETHYL DIHYDROXYPROPYL STEARAMMONIUM CHLORIDE32II08O72AIACT
DMDM HYDANTOINBYR0546TOWIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
SODIUM HYDROXIDE55X04QC32IIACT
TROLAMINE9O3K93S3TKIACT
COAL TARR533ESO2ECACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f6d63b11-1a32-cd80-e053-6394a90a54ce46ae8c1f-5037-46b6-b4e6-1206dfc080ec2023-03-14WarningsExact identifier
spl id: f6d63b11-1a32-cd80-e053-6394a90a54ce
spl set id: 46ae8c1f-5037-46b6-b4e6-1206dfc080ec

Reported adverse events (FAERS/openFDA)#

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