Dr Smiths Diaper Rash description, usages, side effects, indications, overdosage, supplying and lots more!

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Dr Smiths Diaper Rash

Mission Pharmacal Company
Mission Pharmacal Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient Purpose
Zinc Oxide 10% Skin Protectant

Uses

USES

  • helps treat and prevent rash caused by adult incontinence
  • protects chafed skin from wetness

WARNINGS

For external use only

    When using this product
  • do not get into eyes
    Stop use and ask a doctor if
  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

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

DIRECTIONS

  • cleanse the affected area
  • allow to dry
  • shake well before each use
  • spray liberally onto affected area as often as needed

OTHER INFORMATION

  • do not puncture or incinerate, contents under pressure.
  • do not store at temperatures above 120°F
  • store between 15°–30°C (59°–86°F)

INACTIVE INGREDIENTS

Aluminum starch octenylsuccinate, C12-15 alkyl lactate, caprylic/capric triglyceride, cetyl PEG/PPG-10/1 dimethicone, disiloxane, fragrance, hexyl laurate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, magnesium sulfate, methylparaben, octyldodecanol, octyldodecyl xyloside, peg-30 dipolyhydroxystearate, polyglyceryl-4 isostearate, polysorbate 60, polysorbate 80, propylene glycol, propylparaben, sorbitan oleate, squalane, thymol iodide, trans-1,3,3,3-tetrafluorprop-1-ene, triethoxycaprylylsilane, water

To report a serious adverse event or obtain product information, call (210) 696–8400.

Manufactured for:
MISSION PHARMACAL COMPANY
San Antonio, TX 78230 1355

Dr. Smith’s Rash and Skin Spray
NDC 0178–0345–03

Dr Smiths Diaper Rash

Dr Smiths Diaper Rash

Zinc Oxide SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0178-0345
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 10 g

Inactive Ingredients

Ingredient Name Strength
C12-15 ALKYL LACTATE
OCTYLDODECANOL
PEG-30 DIPOLYHYDROXYSTEARATE
propylene glycol
MAGNESIUM SULFATE
DIMETHICONE
water
POLYGLYCERYL-4 ISOSTEARATE
HEXYL LAURATE
THYMOL IODIDE
SODIUM ACRYLOYLDIMETHYLTAURATE
SQUALANE
POLYSORBATE 60
polysorbate 80
SORBITAN MONOOLEATE
METHYLPARABEN
PROPYLPARABEN
1,3,3,3-TETRAFLUOROPROPENE, (1E)-
MEDIUM-CHAIN TRIGLYCERIDES

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0178-0345-03 100 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-04-07


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Be sure to consult your doctor before taking any medication!
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