Label: (FRULI) 75% ALCOHOL DISINFECTANT- alcohol liquid
77442-001-04, view more77442-001-05, 77442-001-06, 77442-001-07
- Packager: Shandong Zhuojian Medical Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Updated May 8, 2020
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SPL UNCLASSIFIED SECTION
This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.
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) consistent with World Health Organization (WHO) recommendations:
- Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
- Glycerol (1.45% v/v).
- Hydrogen peroxide (0.125% v/v).
- Sterile distilled water or boiled cold water.
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
- Active Ingredient(s)
- Do not use
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.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
INGREDIENTS AND APPEARANCE
(FRULI) 75% ALCOHOL DISINFECTANT
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77442-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL in 100 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL in 100 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77442-001-01 60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2020 2 NDC:77442-001-02 100 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2020 3 NDC:77442-001-03 250 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2020 4 NDC:77442-001-04 500 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/01/2020 5 NDC:77442-001-05 2500 mL in 1 CONTAINER; Type 0: Not a Combination Product 05/01/2020 6 NDC:77442-001-06 5000 mL in 1 CONTAINER; Type 0: Not a Combination Product 05/01/2020 7 NDC:77442-001-07 25000 mL in 1 CONTAINER; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/01/2020 Labeler - Shandong Zhuojian Medical Technology Co., Ltd. (419225475) Registrant - Shandong Zhuojian Medical Technology Co., Ltd. (419225475) Establishment Name Address ID/FEI Business Operations Shandong Zhuojian Medical Technology Co., Ltd. 419225475 manufacture(77442-001)