SUNDROPS 75- alcohol gel 
Sunburst Chemicals, Inc.

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SunDrops 75

Active Ingredient

Ethyl Alcohol 60% v/v

Purpose

Skin Sanitizer

Use

To help reduce amount of bacteria on the 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 doctor immediately.

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

Keep out of reach of children.

Directions

  • Place 5 grams or palmful of product in one hand.
  • Spread on hands and run into skin until dry.
  • Place a smaller amount (2.5 grams) in 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, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine

Product Label - 8 fl. oz. Bell Jar with Pump

SUNDROPS 75 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63621-356
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.6 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
WATER (UNII: 059QF0KO0R)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Colorwhite (water white - colorless, crystal clear) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63621-356-208 in 1 BOX10/14/2009
11000 mL in 1 BAG; Type 0: Not a Combination Product
2NDC:63621-356-2512 in 1 BOX10/14/2009
2236.6 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3NDC:63621-356-306 in 1 BOX07/20/201604/30/2022
31000 mL in 1 BAG; Type 0: Not a Combination Product
4NDC:63621-356-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/07/2020
5NDC:63621-356-50473.2 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)10/14/2009
Labeler - Sunburst Chemicals, Inc. (006159339)

Revised: 11/2023
Document Id: 0a5b9639-4ef8-a652-e063-6394a90ac181
Set id: b0623424-939e-4b49-aa99-c1ef22cf0f2d
Version: 8
Effective Time: 20231117
 
Sunburst Chemicals, Inc.