OTC Medication Information: Kroger Waterless Hand Sanitizer Citrus Scent

KROGER WATERLESS HAND SANITIZER CITRUS SCENT- alcohol liquid
The Kroger Company

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 ingredient

Ethyl Alcohol 70% (v/v)

Purpose

Antiseptic

Uses

  • To help reduce bacteria on the skin.

Warnings

For external use only. Flammable. Keep away from source of heat or fire.

When using this product

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

  • irritation or redness develops and lasts.
Keep out of reach of children.
  • In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

  • Put enough product in your palm to cover hands and rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

  • Store at a temperature below 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

Water (Aqua), Fragrance (Parfum), Carbomer, Glycerin, Isopropyl Myristate, Isopropyl Alcohol, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate.

Questons?

1-800-632-6900

Label Copy

Image of the label
(click image for full-size original)

KROGER WATERLESS HAND SANITIZER CITRUS SCENT
ethyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-405
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 700 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
CARBOMER 934
GLYCERIN
ISOPROPYL MYRISTATE
ISOPROPYL ALCOHOL
AMINOMETHYLPROPANOL
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE, DL-
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:30142-405-09 236 mL in 1 BOTTLE, PLASTIC None
2 NDC:30142-405-32 946 mL in 1 BOTTLE, PLASTIC None
3 NDC:30142-405-03 59 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 04/24/2017
Labeler — The Kroger Company (006999528)
Registrant — Apollo Health and Beauty Care Inc. (201901209)
Establishment
Name Address ID/FEI Operations
Apollo Health and Beauty Care Inc. 201901209 manufacture (30142-405)

Revised: 04/2017 The Kroger Company

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.

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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