De La Cruz Sulfur Acne Medication description, usages, side effects, indications, overdosage, supplying and lots more!

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De La Cruz Sulfur Acne Medication

DLC Laboratories, Inc.

De La Cruz Sulfur Ointment 10% Acne Medication


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Sulfur, USP 10%

Purpose

Acne medication

De La Cruz Sulfur Acne Medication Uses

for the treatment of acne

penetrates the pores and dries and clears pimples and blackheads

helps to keep new pimples and blackheads from forming

Warnings

For external use only

When using this product

do not get into eyes

using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin.

If this occurs, only one medication should be used unless directed by a doctor

Stop use and consult a doctor if

excessive skin irritation develops or increases.

KEEP OUT OF THE REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

cleanse the skin thoroughly before applying

cover the entire affected area with a thin layer

leave on for 10 minutes

remove with water

because drying of the skin my occur, start with 1 application daily, then gradually increase to 2 to 3 times daily if needed or as directed by a doctor.

if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredient

polyethylene glycol

Questions?

1-800-858-3889 or www.dlclabs.com

De La Cruz

SULFUR OINTMENT 10%

Acne Medication

2.6 OZ (73.7g)



DE LA CRUZ(R) SULFUR OINTMENT

Dries and clears pimples and blackheads

Helps to keep new pimples and blackheads from forming

Oil-free



NO PARABENS OR ARTIFICIAL COLORS



Manufactured by:

De La Cruz Products

A Division of DLC Laboratories, Inc.

Paramount, CA 90723 USA  

Questions: 1-800-858-3989

(c) DLC www.dlclabs.com

De La Cruz Sulfur Acne Medication

De La Cruz Sulfur Acne Medication

De La Cruz Sulfur Acne Medication

SULFUR OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24286-1525
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SULFUR SULFUR 10 g

Inactive Ingredients

Ingredient Name Strength
POLYETHYLENE GLYCOLS

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24286-1525-2 73.7 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partD part333D 2012-07-27


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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