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OLIKA Hand Sanitizer Orange Blossom / OLIKA Hand Sanitizer Lavender / OLIKA Hand Sanitizer Charcoal / OLIKA Hand Sanitizer Cucumber Basil / OLIKA Hand Sanitizer Mint Citrus

76751-411-01
Dosage form
LIQUID
Labeler
Olika Inc.
Label updated
2021-12-10
Retrieved
2026-09-07
Active ingredients
ALCOHOL
View original label and images on DailyMed ↗
Label information

These products are hand sanitizers manufactured according to the 1994 tentative final monograph for antiseptics with additional guidance taken from subsequent rule makings and guidances.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation).

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (65%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (4.2% v/v).
  3. Aloe Barbadensis Leaf Extract.
  4. Sterile distilled water or boiled cold water.
  5. Fragrance

The finished product formulation underwent third party efficacy testing (kill study) to confirm efficacy and product potency.

The hand sanitizer come in 6 different scents. Fragrance free (submitted separately NDC 76751-211), Lavender (NDC 76751-611), Orange Blossom (NDC 76751-511), Mint Citrus (NDC 76751-111), Charcoal (NDC 76751-311) and Cucumber Basil (NDC 76751-411).

Active Ingredient(s)

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Warnings

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

Do not use
  • in children less than 2 months of age
  • on open skin wounds
Label information

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

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Label information

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Label information

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other information
  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)
Use

Helps reduce bacteria on skin.

Directions
  • Remove nozzel bead.
  • Spray liquid in hands and rub until dry.
  • Use as often as needed.
Inactive Ingredients

Inactive Ingredients for NDCs 76751-111-01; 76751-311-01; 76751-411-01; 76751-511-01; 76751-611-01

  • Aloe Barbadensis Leaf Extract
  • Fragrance (Essential Oil Blend)
  • Glycerin
  • Water
Primary container spray bottle bottom label
Bottle printed label on bottom

Bottom label for primary container spray bottle for all scents:

76751-411-01 Prinicipal Display Panel and information panel image
76751-411-01

76751-411-01 30 mL

76751-111-01 Prinicipal Display Panel and information Panel
111-01

30 mL NDC 76751-111-01

76751-311-01 Image Principal Display Panel & Information Panel
76751-311-01

30 mL NDC 76751-311-01

76751-511-01 Principal Display panel and information panel
511-01

30mL NDC 76751-511-01

76751-111-02 Principal Display and Information Panel
111-02

20 mL NDC 76751-111-02

76751-311-02 Principal Display and Information Panel
311-02

20mL NDC 76751-311-02

76751-611-02 PRINCIPAL DISPLAY PANEL AND INFORMATION LABEL
611-02

20 mL NDC 76751-611-02

76751-411-02 PRINCIPAL DISPLAY PANEL AND INFORMATION PANEL
411-02

20 mL NDC 76751-411-02

76751-111-03 PRINCIPAL DISCPLAY PANEL AND INFORMATION PANEL
111-03

90 mL NDC 76751-111-03

76751-611-03 PRINCIPAL DISPLAY PANEL AND INFORMATION PANEL
611-30 90mL

90 mL NDC 76751-611-03

76751-311-03 PRINCIPAL DISPLAY PANEL AND INFORMATION PANEL
311-03

90 mL NDC 76751-311-03

76751-411-03 PRINCIPAL DISPLAY PANEL AND INFORMATION PANEL
411-03

90 mL NDC 76751-411-03

76751-511-03 PRINCIPAL DISPLAY PANEL AND INFORMATON PANEL
511-03

90 mL NDC 76751-511-03

76751-611-01 PRINCIPAL DISPLAY PANEL AND INFORMATION PANEL
611-01

30mL NDC 76751-611-01

76751-511-02 PRINCIPAL DISPLAY PANEL AND INFORMATION PANEL
511-02

20 mL NDC 76751-511-02

DailyMed Set ID: a40f4421-88f2-0fe2-e053-2995a90a69b7 · Version 5
NDC: 76751-111, 76751-311, 76751-411, 76751-511, 76751-611