APOLLO INSTANT HAND SANITIZER- instant hand sanitizer gel 
Sbu Group L.P.

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.

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apollo Instant Hand Sanitizer

Active ingredient

Alcohol 75%v/v

Purpose

Antiseptic

Uses:

Hand sanitizer to help decrease bacterial on the skin, when water, soap& towel are not available.

Recommended for repeated use.

Warnings

For external use only. Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

When using this product,

Avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor

If redness or irritation develop and persist for more than 72 hours

Keep out of reach of children.

Children must be supervised in use of this product.

Directions

Place enough product into your palms and thoroughly spread on both hands.

Rub into skin until dry.

Other information

Store below 110℉（43℃）

May discolor certain fabrics or surfaces.

Inactive ingredients

Water, Glycerin, Triethanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer.

Package Label

apollo

Instant Hand Sanitizer

Anti Bacterial

Contains 75 % Alcohol

2 FL OZ (60ml)

Kills 99% Germs

NDC: 78303-001-01

60ML Label

Package Label

apollo

Instant Hand Sanitizer

Anti Bacterial

Contains 75 % Alcohol

1.29 Gallons

5,000 ML

Kills 99% Germs

NDC: 78303-001-02

5000ML Label

APOLLO INSTANT HAND SANITIZER 
instant hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78303-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78303-001-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product05/06/2020
2NDC:78303-001-025000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/06/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/06/2020
Labeler - Sbu Group L.P. (841530095)
Registrant - GUANGZHOU XUELEI COSMETIC CO.,LTD. (526885026)
Establishment
NameAddressID/FEIBusiness Operations
GUANGZHOU XUELEI COSMETIC CO.,LTD.526885026manufacture(78303-001) , pack(78303-001) , label(78303-001)

Revised: 11/2021
Document Id: d0524f5c-09e4-c7ff-e053-2a95a90a04de
Set id: a6976e49-aa6d-0aaf-e053-2a95a90aa065
Version: 4
Effective Time: 20211108
 
Sbu Group L.P.