HAND SANITIZER WITH ALOE VERA- alcohol gel 
Pharmco Laboratories, Inc.

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Hand Sanitizer with aloe vera

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin

Warnings

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

Do not use

  • in children less that 2 months of age
  • on open wounds

When using this product, keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Discontinue use if irritation or redness develops.

If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children. If swallowed get medical help or call a poison control center immediately.

Directions

Other Information

Inactive Ingredients

Water, Glycerin, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Citric Acid, Sodium Hydroxide

Manufactured by:
Pharmco Laboratories, Inc.
3520 South St. Titusville, FL 32780

PRINCIPAL DISPLAY PANEL - 59 mL Tube Label

pharmco
MANUFACTURER OF PREMIUM SKIN CARE PRODUCTS

HAND
SANITIZER
with aloe vera

2 fl oz. (59 mL)

PRINCIPAL DISPLAY PANEL - 59 mL Tube Label
HAND SANITIZER WITH ALOE VERA 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58400-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
Aloe Vera Leaf (UNII: ZY81Z83H0X)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58400-010-0259 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2020
2NDC:58400-010-04125 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
3NDC:58400-010-08228 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2020
4NDC:58400-010-30885 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
5NDC:58400-010-013780 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
6NDC:58400-010-55207000 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM00305/01/2020
Labeler - Pharmco Laboratories, Inc. (096270814)
Establishment
NameAddressID/FEIBusiness Operations
Pharmco Laboratories, Inc.096270814MANUFACTURE(58400-010) , LABEL(58400-010) , PACK(58400-010)

Revised: 1/2024
Document Id: 7110d632-21f2-48ea-bec0-f83c2649dc90
Set id: 72f635f2-17a4-4c2e-b45c-a70816bc9f4b
Version: 2
Effective Time: 20240111
 
Pharmco Laboratories, Inc.