Sebrx Topical Analgesic description, usages, side effects, indications, overdosage, supplying and lots more!

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Sebrx Topical Analgesic

Goodier Cosmetics LP
Goodier Cosmetics LP


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Sebrx Retail 2 fl oz Topical Analgesic

    sebRx

    Oil Control Gel
    Topical Analgesic

    2 fl oz / 60 ml

Active ingredient

    Active Ingredient
    Diphenhydramine HCl 2%
    Purpose
    External Analgesic

Purpose

    For the temporary relief
    of pain and itching associated
    with minor skin irritations.

Uses

    Uses • For the temporary relief
    of pain and itching associated
    with minor skin irritations.

    Warnings
    When using this product

    • Avoid contact with eyes.

    Stop use and ask a physician if
    • Condition worsens.
    • Symptoms persist for more
    than 7 days.
    • Symptoms clear up and
    occur again within a few days.

    For external use only.

    Keep this and all drugs out of
    reach of children. If swallowed,
    get medical help or contact a
    Poison Control Center right away.

    Directions • Shake well
    before use. Adults/children 2
    years of age and older:

    • Dispense 4 pumps of
    product into palm of hand.
    • Apply to affected area
    2 times daily.
    Children under 2 years of age:
    • Consult a physician.

    Other Information
    Store at 68-77°F (20-25°C)

    Inactive Ingredients
    Water (Aqua), SD Alcohol 40
    (Alcohol Denat.), Ethoxydiglycol,
    Sodium Lactate, Cucurbita Pepo
    (Pumpkin) Seed Extract,
    Zingiber Officinalis (Ginger)
    Root Extract, Cinnamomum
    Cassia Bark Extract, Poterium
    Officinale (Burnet) Root Extract,
    Hydroxyethylcellulose, Butylene
    Glycol, Phenoxyethanol, Salicylic
    Acid, Citric Acid


    Dist. By Revision, Inc
    Dallas, TX 75247 Made In USA

Sebrx Topical Analgesic

Sebrx Topical Analgesic

Diphenhydramine Hydrochloride GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10477-3410
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 2 g

Inactive Ingredients

Ingredient Name Strength
water
DIETHYLENE GLYCOL MONOETHYL ETHER
sodium lactate
PUMPKIN SEED
GINGER
CHINESE CINNAMON
SANGUISORBA OFFICINALIS ROOT
HYDROXYETHYL CELLULOSE (2000 MPA.S FOR 1% AQUEOUS SOLUTION)
BUTYLENE GLYCOL
PHENOXYETHANOL
Salicylic Acid
ANHYDROUS CITRIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10477-3410-1 60 in 1 BOTTLE, PLASTIC
2 60 in 1 BOTTLE, PLASTIC
3 NDC:10477-3410-2 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2008-02-01


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Be sure to consult your doctor before taking any medication!
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