amazon basics maximum strength dandruff

Manufacturer
AMAZON.COM SERVICES LLC | Garcoa, Inc. | SV Labs Toronto Corporation
Effective date
2024-02-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:42:28

Label at a glance#

Productamazon basics maximum strength dandruff Anti-dandruff
Active ingredientSelenium sulfide
Label structure11 sections

Dosage and administration

shake well. wet hair. massage onto scalp. rinse. repeat if desired. for best results, use at least twice a week or as directed by a doctor. for maximum dandruff control, use every time you shampoo.

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Selenium sulfide 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

WARNINGS SECTION

For external use only.

OTC - ASK DOCTOR SECTION

Ask a doctor before using this product if condition covers a large area of the body.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve after regular use of this product as directed.
  • if condition covers a large area of the body.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well.
  • wet hair.
  • massage onto scalp.
  • rinse.
  • repeat if desired.
  • for best results, use at least twice a week or as directed by a doctor.
  • for maximum dandruff control, use every time you shampoo.

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, ammonium lauryl sulfate, ammonium laureth sulfate, distearyl phthalic acid amide, cocamide MEA, fragrance, titanium dioxide, dimethicone, hydroxypropyl methylcellulose, citric acid, sodium lauroyl lactylate, aloe barbadensis leaf juice, sodium citrate, sodium chloride, phenoxyethanol, methylchloroisothiazolinone, methylisothiazolinone, blue 1, yellow 10, ext. violet 2.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-567-8600

SPL UNCLASSIFIED SECTION

Distributed by: Amazon.com Services LLC
Seattle, WA 98109, 1-877-485-0385

PRINCIPAL DISPLAY PANEL - 325 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

amazon basics

maximum strength

dandruff
shampoo

Selenium Sulfide 1%
Moisturizing with Aloe
For the Relief of Symptoms
Associated with Dandruff

Compare to Selsun Blue®
Selenium Sulfide
Anti-Dandruff Shampoo*

11 FL OZ (325 mL)

P-03841
05-4698

PRINCIPAL DISPLAY PANEL - 325 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 325 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204642selenium sulfide 1 % Medicated ShampooPSN2
204642selenium sulfide 10 MG/ML Medicated ShampooSCD2
204642selenium sulfide 1 % Lotion ShampooSY2
204642selenium sulfide 1 % Medicated ShampooSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72288-551-01amazon basics maximum strength dandruffAnti-dandruff325 mL in 1 BOTTLESHAMPOO3252

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72288-55172288-551-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-02-26full-release2026-06-01 00:09:05

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
amazon basics maximum strength dandruff Anti-dandruffSELENIUM SULFIDEAMAZON.COM SERVICES LLC194e4c51-ff7b-4def-a71d-efa5dfca3efd2024-02-26WarningsExact identifier
ndc (package): 72288-551-01
ndc (product): 72288-551
ndc11 (package): 72288055101
spl id: 01383804-b17a-42da-b4f1-605a7b0b60be
spl set id: 194e4c51-ff7b-4def-a71d-efa5dfca3efd

Reported adverse events (FAERS/openFDA)#

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