FAMILY Wellness EVERYDAY CLEAN 2 IN 1 DANDRUFF PLUS CONDITIONER Anti-Dandruff

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: FAMILY Wellness EVERYDAY CLEAN 2 IN 1 DANDRUFF PLUS CONDITIONER Anti-Dandruff
Generic name: PYRITHIONE ZINC
Manufacturer: FAMILY DOLLAR SERVICES INC
Product type: HUMAN OTC DRUG
SPL set ID: 220955ec-592c-421f-9f4e-545ff3843ee0
SPL ID: 562a78e5-a922-4aaa-b6a2-ddd1c047b103
Version: 3
Effective date: 2024-10-21
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:47

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M032	openfda.application_number
brand name		FAMILY Wellness EVERYDAY CLEAN 2 IN 1 DANDRUFF PLUS CONDITIONER Anti-Dandruff	openfda.brand_name
generic name		PYRITHIONE ZINC	openfda.generic_name
manufacturer name		FAMILY DOLLAR SERVICES INC	openfda.manufacturer_name
ndc	package	55319-386-01	openfda.package_ndc
ndc	package	55319-386-02	openfda.package_ndc
ndc	package	55319-386-03	openfda.package_ndc
ndc	product	55319-386	openfda.product_ndc
ndc11	package	55319038601	derived:openfda.package_ndc
ndc11	package	55319038603	derived:openfda.package_ndc
ndc11	package	55319038602	derived:openfda.package_ndc
rxcui		209884	openfda.rxcui
spl id		562a78e5-a922-4aaa-b6a2-ddd1c047b103	id
spl set id		220955ec-592c-421f-9f4e-545ff3843ee0	set_id
unii		R953O2RHZ5	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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