SunDrops 73 description, usages, side effects, indications, overdosage, supplying and lots more!

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SunDrops 73

Sunburst Chemicals, Inc.

SunDrops 73


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Ethyl Alcohol 65% v/v

Purpose

Skin Sanitizer

Use

To help reduce the amount of bacteria on skin

Warnings

Flammable. Keep away from fire or flame.

For external use only. If swallowed seek medical attention.

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

KEEP OUT OF REACH OF CHILDREN.

Directions

  • Pump a small amount of foam into palm of hand.
  • Spread on hands and rub into skin until dry.
  • Pump a smaller amount (2.5 grams) into one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

Inactive Ingredients

Water, DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin

PRINCIPAL DISPLAY PANEL - Label

SUNBURST CHEMICALS

SunDrops
73

Contains 6 Bottles
Net Contents Each 16 fl. oz. (1 pt.) 500 mL
Total Net Volume 96 fl. oz. (3 qt.) 3 L

SunDrops 73

SunDrops 73

Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63621-355
Route of Administration CUTANEOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 0.65 mL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63621-355-50 500 in 1 BOTTLE, PUMP
2 NDC:63621-355-55 1000 in 1 BAG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2009-10-14


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