Head Remedy Dandruff Conditioner
- Manufacturer
- KPSS, Inc.
- Effective date
- 2010-08-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 22:25:49
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: Zinc Pyrithione 1.0%
OTC - PURPOSE SECTION
Purpose: Antidandruff
INDICATIONS & USAGE SECTION
Use: Controls dandruff and flaking for a healthy scalp.
WARNINGS SECTION
Warnings: For external use only.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have: seborrheic dermatitis that covers a large area of the body.
OTC - WHEN USING SECTION
When using this product: do not get in eyes. If contact occurs, rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if: condition worsens or does not improve after regular use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep Out of Children's Reach: If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions: Apply small amount on shampooed hair. Massage into wet hair and scalp. Leave in 2 minutes and rinse. For best results, use at least 2 times a week.
OTC - QUESTIONS SECTION
Distributed by KPSS Inc., Linthicum Heights, MD 21090 USA, 1-800-342-5567
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
MM1: 8oz_dandruff_conditioner_label.jpg
INACTIVE INGREDIENT SECTION
water, cetearyl alcohol, isopropyl palmitate, stearamidopropyl dimethylamine, phenethyl dimethicone, mineral oil, lactic acid, panthenol, butylene glycol, propylene glycol, glucose, Foeniculum vulgare (Fennel) fruit extract, Melissa officinalis (Balm) extract, Salvia officinalis (Sage) extract, Rosmarinus officinalis (Rosemary) extract, Urtica dioica (Nettle) extract, Equisetum arvense (Horsetail) extract, Humulus lupulus (Hops) extract, Chamomilla recutita (Matricaria) flower extract, caramel, sorbitol, sodium benzoate, potassium sorbate, DMDM Hydantoin, phenoxyethanol, tartaric acid, methylparaben, propylparaben, isobutylparaben, ethylparaben, butylparaben, fragrance, blue 1
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1043244 | head & shoulders 1 % Medicated Shampoo | PSN | 2 |
| 209884 | zinc pyrithione 1 % Medicated Shampoo | PSN | 2 |
| 1043244 | zinc pyrithione 10 MG/ML Medicated Shampoo [Head & Shoulders] | SBD | 2 |
| 209884 | zinc pyrithione 10 MG/ML Medicated Shampoo | SCD | 2 |
| 1043244 | Head & Shoulders 1 % Medicated Shampoo | SY | 2 |
| 1043244 | Head & Shoulders 10 MG/ML Medicated Shampoo | SY | 2 |
| 209884 | zinc pyrithione 1 % Medicated Conditioner | SY | 2 |
| 209884 | zinc pyrithione 1 % Medicated Shampoo | SY | 2 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 25237-0516-1 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-d071-621f-e053-dbdaa90a74ad | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 25237-0516-1 | Head Remedy Dandruff Conditioner | 249.4 g in 1 BOTTLE | EMULSION | 249.4 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 25237-0516 | HEAD REMEDY DANDRUFF CONDITIONER (PYRITHIONE ZINC) EMULSION [KPSS, INC.] | 2 | Legacy NDC, 1 package rows | 20100915_2c00ade9-b7e7-4005-933a-bde9572cc437.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| PYRITHIONE ZINC | ACTIVE INGREDIENT | R953O2RHZ5 | 2 | |
| PYRITHIONE ZINC | ACTIVE MOIETY | R953O2RHZ5 | 2 |
Products#
Every source-derived product name is available through these pages.
- Head Remedy Dandruff Conditioner
- PYRITHIONE ZINC
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 25237-0516 | 25237-0516-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PYRITHIONE ZINC | R953O2RHZ5 | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| c38bb28f-113e-48cb-8e52-509ccb9ecc09 | 2c00ade9-b7e7-4005-933a-bde9572cc437 | 2010-08-19 | Warnings | c38bb28f-113e-48cb-8e52-509ccb9ecc09 2c00ade9-b7e7-4005-933a-bde9572cc437 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
