Indications and uses
controls the symptoms of dandruff, seborrheic dermatitis, and psoriasis.
EQUATE ANTI DANDRUFF
- Manufacturer
- WAL-MART STORES INC | APOLLO HEALTH AND BEAUTY CARE
- Effective date
- 2016-02-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:45:13
Label at a glance#
ProductEQUATE ANTI DANDRUFF
Active ingredientSALICYLIC ACID
Label structure7 sections
Dosage and administration
for best results, use twice a week or as directed by a doctor. wet hair, massage onto scalp for several minutes, and then rinse. repeat if desired.
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Salicylic Acid 2%
Purpose
Anti-Dandruff/Anti-Seborrheic Dermatitis/Anti-Psoriasis
Uses
controls the symptoms of dandruff, seborrheic dermatitis, and psoriasis.
Warnings
For external use only.
Ask a doctor before use if you have
a condition that covers a large area of the body.
When using this product
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- for use on color treated or permed hair, rinse thoroughly.
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.
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- for best results, use twice a week or as directed by a doctor.
- wet hair, massage onto scalp for several minutes, and then rinse.
- repeat if desired.
Inactive ingredients
Water (Aqua), Sodium Laureth Sulfate, Acrylates Crosspolymer-4, Cocamide MEA, Sodium Cocoyl Sarcosinate, Glycol Distearate, Polyquaternim-7, Fragrance (Parfum), Sodium Chloride, Sodium Hydroxide, Tetrasodium EDTA, BHT, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090).
Questions or Comments?
1-888-287-1915
Label Copy
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49035-450-07 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-075d-f424-e053-dadaa90a57ce | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49035-450-07 | EQUATE ANTI DANDRUFF | 207 mL in 1 BOTTLE, PLASTIC | SHAMPOO | 207 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- EQUATE ANTI DANDRUFF
- SALICYLIC ACID
- WATER
- SODIUM LAURETH-3 SULFATE
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
- COCO MONOETHANOLAMIDE
- SODIUM COCOYL SARCOSINATE
- GLYCOL DISTEARATE
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)
- SODIUM CHLORIDE
- SODIUM HYDROXIDE
- EDETATE SODIUM
- BUTYLATED HYDROXYTOLUENE
- METHYLCHLOROISOTHIAZOLINONE
- METHYLISOTHIAZOLINONE
- FD&C BLUE NO. 1
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49035-450 | 49035-450-07 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 535fd575-1c19-4f26-a890-c8327b31e31e | cd3dc6b0-cbbc-4a26-b2b9-666d794005d5 | 2016-02-29 | Warnings | 535fd575-1c19-4f26-a890-c8327b31e31e cd3dc6b0-cbbc-4a26-b2b9-666d794005d5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.