FDA.reportPublic FDA data

Crawford Dandruff

Manufacturer
Keefe Group
Effective date
2021-08-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:37:24

Label at a glance#

ProductCrawford Dandruff
Active ingredientPYRITHIONE ZINC
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Pyrithione zinc 0.5%

OTC - PURPOSE SECTION

Purpose

Anti dandruff

INDICATIONS & USAGE SECTION

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

WARNINGS SECTION

Warnings using this product
For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions: For maximum dandruff control, use at least twice a week. Wet hair, massage through hair and scalp, rinse and repeat if desired.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:

Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Glycol Distearate, Cocamidopropyl Betaine, Polyquaternium-7, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue #1

SPL UNCLASSIFIED SECTION

Manufactured for

Crawford Supply • St. Louis, MO 63132

PRODUCT OF CANADA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Crawford

Dandruff Shampoo

Clears Hair of Dandruff Flakes

4 fl. oz. (118 mL)

Crawford Dandruff ShampooCrawford Dandruff Shampoo

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51870-005-042021-08-23C16284748780-1c7ccaba7-211e-fd44-e053-dadaa90aa01bCrawford Dandruff Shampoo
51870-005-122021-08-23C16284748780-1c7ccaba7-211e-fd44-e053-dadaa90aa01bCrawford Dandruff Shampoo
51870-005-042021-07-23C16284748780-1c7ccaba7-211e-fd44-e053-dadaa90aa01bCrawford Dandruff Shampoo
51870-005-122021-07-23C16284748780-1c7ccaba7-211e-fd44-e053-dadaa90aa01bCrawford Dandruff Shampoo

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51870-00551870-005-04, 51870-005-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
GLYCOL DISTEARATE13W7MDN21WIACT
SODIUM CHLORIDE451W47IQ8XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)0L414VCS5YIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB

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
d0d64cd6-77c9-1188-e053-2a95a90ae2ee8810c182-08c7-7c38-e053-2a95a90a8d662021-11-15WarningsExact identifier
spl set id: 8810c182-08c7-7c38-e053-2a95a90a8d66

Reported adverse events (FAERS/openFDA)#

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