Skin Block Extra Strength Hand Sanitizer

Skin Block Extra Strength Hand Sanitizer by

Drug Labeling and Warnings

Skin Block Extra Strength Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Charter Oak Development Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SKIN BLOCK EXTRA STRENGTH HAND SANITIZER- benzalkonium chloride liquid 
Charter Oak Development Corporation

----------

Skin Block Extra Strength Hand Sanitizer

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic Hand Sanitizer

Uses:

Hand and skin anti-microbial to help decrease pathogens (bacteria & germs) on the skin. Recommended for repeated use

Warnings:

Do not freeze  For external use only 

Do not use 

in ears or mouth.

When using this product,

  • avoid contact with the 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 should be supervised when using this product.

Directions:

Apply a small amount into palms and spread on both hands. Rub into skin until dry. Repeat as necessary.

Inactive Ingredients:

Water, Polyaminopropyl biguanide, 1-Octadecanaminum NN dimethyl (3- trimethoxysily) propyl chloride, C12-15 Pareth 12, Caprylyl Glucoside, Sodium Benzoate, Glycerin, Aloe Barbadensis Leaf Juice Extract, Citric Acid

Package Labeling:50ml

Bottle

Package Labeling:200ml

Bottle2

Package Labeling:

Bottle3

SKIN BLOCK EXTRA STRENGTH HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80254-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80254-000-0050 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/202012/31/2024
2NDC: 80254-000-01200 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/202012/31/2024
3NDC: 80254-000-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/202012/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/01/202012/31/2024
Labeler - Charter Oak Development Corporation (076200437)

Revised: 1/2025
Document Id: 2cd80b76-788e-d75e-e063-6394a90af3b8
Set id: ae7ef91c-261a-ca13-e053-2995a90a54a7
Version: 3
Effective Time: 20250129