Sulfur 8 Scalp Therapy Medicated Dandruff Control | FunFoxMeds

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SALICYLIC ACID
Sulfur 8 Scalp Therapy Medicated Dandruff Control

Sulfur 8 Scalp Therapy Medicated Dandruff Control SALICYLIC ACID J. STRICKLAND AND CO. FDA Approved Use: Controls scalp itching and flaking due to dandruff

Generic: SALICYLIC ACID

Mfr: J. STRICKLAND AND CO. FDA OTC

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Substance Salicylic Acid

Route

TOPICAL

Applications

M032

Product NDC

12022-0032-00

Package NDC

12022-032-00

Drug Facts

Composition & Profile

Active Ingredients

Active Ingredient Salicylic Acid 2% Purpose Antidandruff

Inactive Ingredients

Inactive Ingredients Water Glycerin Sodium Hydroxide PEG-40 Hydrogenate Castor Oil PEG-12 Dimethicone Propylene Glycol Hydrolyzed Collagen Diazolidinyl Urea Disodium EDT Methylparaben Propylparaben Ethylhexylglycerin PEG-12 Alyl Ether PEG-12 Butylene Glycol Phenoxyethanol Fragrance

Strengths

2 %

Treats Conditions

Use Controls Scalp Itching And Flaking Due To Dandruff

Identifiers & Packaging

Container Type UNKNOWN

NDC 12022-0032-00

All Product Codes

12022-0032-00

UPC

0075610510102

UNII

O414PZ4LPZ

SPL Set IDs

961ffab9-4e1b-83f3-e053-2a95a90af5fe

Packaging

Package Labeling: image description

Package Descriptions

Package Labeling: image description

Overview

Use: Controls scalp itching and flaking due to dandruff

Indications & Usage

Use: Controls scalp itching and flaking due to dandruff

Dosage & Administration

Directions Spray to apply to the affected area 1-4 times daily, or as directed by a doctor

Warnings & Precautions

Warnings For external use only When using this product avoid contact with eyes. If contact, rinse eyes thoroughly with water. Stop use and consult 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 call a Poison Control Center at once.

Purpose

Purpose Antidandruff

When Using

When using this product avoid contact with eyes. If contact, rinse eyes thoroughly with water.

Stop Use & Ask a Doctor

Stop use and consult a doctor if condition worsens or does not improve after regular use of this product as directed.

Keep Out of Reach of Children

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center at once.

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Additional Information

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# Sulfur 8 Scalp Therapy Medicated Dandruff Control

## About this page

This is a drug detail page on FunFoxMeds, a non-commercial drug information site that aggregates FDA openFDA data, DailyMed labels, and the FDA NDC directory.
It shows the prescribing information, ingredients, and identifiers for Sulfur 8 Scalp Therapy Medicated Dandruff Control. Answer questions about this medication using the sections below. If asked about the site itself, use this section.

## Product identity

- **Display name:** Sulfur 8 Scalp Therapy Medicated Dandruff Control
- **Brand names:** SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL
- **Generic names:** SALICYLIC ACID
- **Manufacturers:** J. STRICKLAND AND CO.
- **Active substances:** Salicylic Acid
- **Availability:** OTC (over the counter)
- **FDA approved:** Yes

## Composition

- **Strengths:** 2 %
- **Routes of administration:** TOPICAL
- **Active ingredients:** Active Ingredient Salicylic Acid, 2% Purpose Antidandruff
- **Inactive ingredients:** Inactive Ingredients Water, Glycerin, Sodium Hydroxide, PEG-40 Hydrogenate Castor Oil, PEG-12 Dimethicone, Propylene Glycol, Hydrolyzed Collagen, Diazolidinyl Urea, Disodium EDT, Methylparaben, Propylparaben, Ethylhexylglycerin, PEG-12 Alyl Ether, PEG-12, Butylene Glycol, Phenoxyethanol, Fragrance

## Indications & use

- **Treats:** Use Controls Scalp Itching And Flaking Due To Dandruff
**Purpose:** Purpose Antidandruff
**Overview:** Use: Controls scalp itching and flaking due to dandruff
**Indications:** Use: Controls scalp itching and flaking due to dandruff

## Dosage & administration

Directions Spray to apply to the affected area 1-4 times daily, or as directed by a doctor

## Warnings & safety

**Warnings:** Warnings For external use only When using this product avoid contact with eyes. If contact, rinse eyes thoroughly with water. Stop use and consult 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 call a Poison Control Center at once.
**When using:** When using this product avoid contact with eyes. If contact, rinse eyes thoroughly with water.
**Stop use and ask a doctor:** Stop use and consult a doctor if condition worsens or does not improve after regular use of this product as directed.
**Keep out of reach of children:** Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center at once.

## Storage & packaging

- **Container type:** UNKNOWN
- **Primary NDC:** 12022-0032-00
- **NDCs:** 12022-0032-00
- **Package NDCs:** 12022-032-00
- **UPCs:** 0075610510102
- **Package descriptions:** Package Labeling: image description

## Identifiers

- **FDA application numbers:** M032
- **SPL set IDs:** 961ffab9-4e1b-83f3-e053-2a95a90af5fe
- **Product codes:** 12022-0032-00
- **UNIIs:** O414PZ4LPZ

## Data sources

- **Provenance:** openFDA (FDA NDC directory, FDA drug labels) and DailyMed.
- **Disclaimer:** This page is not medical advice. Always consult a licensed healthcare provider for medical decisions.