SunDrops 73 by Sunburst Chemicals, Inc.

SunDrops 73 by

Drug Labeling and Warnings

SunDrops 73 by is a Otc medication manufactured, distributed, or labeled by Sunburst Chemicals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SUNDROPS 73- alcohol soap 
Sunburst Chemicals, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

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

Principal Display Panel - Label
SUNDROPS 73 
alcohol soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 63621-355
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol650 mL  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)  
Product Characteristics
Colorwhite (water white - colorless, dispensed as white foam) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 63621-355-506 in 1 BOX10/14/200903/18/2020
10.500 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC: 63621-355-558 in 1 BOX10/14/200903/18/2020
21 L in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/14/200903/18/2020
Labeler - Sunburst Chemicals, Inc. (006159339)

Revised: 3/2020
Document Id: 7cf24358-8839-4c03-8377-299d5185e65c
Set id: a188129a-ab1d-4ddf-a1d0-9a0eb04b60dc
Version: 4
Effective Time: 20200318
 
Sunburst Chemicals, Inc.