NDC 73976-1330

Santotizer

Hand Santizer Solution

Santotizer is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Santolubes Llc. The primary component is Alcohol.

• Product ID: 73976-1330_a18cef50-abe0-a416-e053-2a95a90a83de
• NDC: 73976-1330
• Product Type: Human Otc Drug
• Proprietary Name: Santotizer
• Generic Name: Hand Santizer Solution
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2020-03-30
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333A
• Labeler Name: Santolubes LLC
• Substance Name: ALCOHOL
• Active Ingredient Strength: 80 L/100L
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 73976-1330-1

3.6 L in 1 PAIL (73976-1330-1)

• Marketing Start Date: 2020-03-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73976-1330-1 [73976133001]

Santotizer LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-30

NDC 73976-1330-2 [73976133002]

Santotizer LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-30

NDC 73976-1330-3 [73976133003]

Santotizer LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-30

NDC 73976-1330-4 [73976133004]

Santotizer LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-03-30

Drug Details

Active Ingredients

Ingredient	Strength
ALCOHOL	80 L/100L

OpenFDA Data

• SPL SET ID: a18cef50-abdf-a416-e053-2a95a90a83de
• Manufacturer:
  • Santolubes LLC
• UNII:
  • 3K9958V90M
• RxNorm Concept Unique ID - RxCUI:
  • 1039339