LANDRUM INSTANT HAND SANITIZER: Package Insert and Label Information

LANDRUM INSTANT HAND SANITIZER- ethanol gel
Kentucky Technology LLC.

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:

Ethanol (60% v/v)

Purpose:

Anti-Microbial Hand Sanitizer

Uses

  • Helps reduce bacteria that potentially can cause disease
  • Helps prevent cross contamination by hand contact
  • Recommended for repeated use

Warnings

  • For external use only
  • Flammable, keep away from fire, heat, or flame
  • Keep out of reach of children.
  • Do not use near eyes
  • In case of eye contact flush with water for 15 minutes
  • If irritation persists stop use of product and get medical attention
  • In case of accidental ingestion seek medical attention or contact a poison control center immediately.

Directions

  • Use no water or towels
  • Apply appropriate amount of product to palm of hand
  • Rub until hands are completely covered
  • Agitate lightly until dry
  • Let air dry for 15 seconds
  • Do not rinse or wipe with towel.

Other Information

  • Store in a cool dry place below 104° F.

Inactive Ingredients

Water, Carbomer, Triethanolamine, PEG-75 Lanolin, Aloe Vera Gel, Fragrance.

Principal Display Panel

Principal Display Panel – Bottle Label

LANDRUM CHEMICAL INDUSTRIES

LANDRUM INSTANT HAND SANITIZER

  • Enhanced with Moisturizers
  • Kills disease causing germs within seconds
  • Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
  • Assists with OSHA Bloodborne Pathogen Standard Compliance

For Hospital and Professional Use Only See Drug Facts panel for additional information

Figure
(click image for full-size original)
LANDRUM INSTANT HAND SANITIZER
ethanol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68088-515
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ethanol (ethanol) ethanol 600 mL in 1000 mL
Inactive Ingredients
Ingredient Name Strength
water
carbomer homopolymer type C
aloe
trolamine
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68088-515-62 237 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333 05/21/2010
Labeler — Kentucky Technology LLC. (139036375)
Establishment
Name Address ID/FEI Operations
Canberra Corporation 068080621 MANUFACTURE

Revised: 05/2010 Kentucky Technology LLC.

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