OTC Medication Information: Raon Hand Sanitizing Wipes

RAON HAND SANITIZING WIPES- benzalkonium chloride liquid
Liz Corporation Co., Ltd

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.

Active ingredients

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Use

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only : hands

Flammable. Keep away from heat and flame.

When using this product

  • Keep out of eyes. In case of contact with eyse, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.

Stop use and ask a doctor if

  • irritation and redness develop skin irritation or rash develops
  • condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wipe hands thoroughly with product and allow to dry
  • Discard wipe in trash. Do not flush.

Inactive ingredients

Water, Glycerin, Polysorbate 80, Sodium Benzoate, Citric Acid, Maltodextrin, Aloe Barbadensis Leaf Juice Powder, Fragrance, Tocopheryl Acetate

Package Label

79487-203-01
(click image for full-size original)
79487-203-02
(click image for full-size original)

RAON HAND SANITIZING WIPES
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79487-204
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.1 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
CITRIC ACID MONOHYDRATE
MALTODEXTRIN
GLYCERIN
SODIUM BENZOATE
ALOE VERA LEAF
POLYSORBATE 80
.ALPHA.-TOCOPHEROL ACETATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79487-204-01 279 g in 1 POUCH None
2 NDC:79487-204-02 93 g in 1 POUCH None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 02/20/2021
Labeler — Liz Corporation Co., Ltd (694803273)
Registrant — Liz Corporation Co., Ltd (694803273)
Establishment
Name Address ID/FEI Operations
Liz Corporation Co., Ltd 694803273 manufacture (79487-204)

Revised: 02/2021 Liz Corporation Co., Ltd

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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