Label: HAND SANITIZER- alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 75594-021-01, 75594-021-02, 75594-021-03, 75594-021-04, view more75594-021-05, 75594-021-06, 75594-021-07, 75594-021-08 - Packager: Commercial Beverage Concepts, LLC
- This is a repackaged label.
- Source NDC Code(s): 77034-002
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated July 28, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
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)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75594-021(NDC:77034-002) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 L in 1 L Inactive Ingredients Ingredient Name Strength AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371) ISOPROPYL ALCOHOL (UNII: ND2M416302) METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75594-021-01 0.237 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/28/2020 2 NDC:75594-021-02 0.473 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/28/2020 3 NDC:75594-021-03 0.946 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/28/2020 4 NDC:75594-021-04 1.89 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/28/2020 5 NDC:75594-021-05 3.78 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/28/2020 6 NDC:75594-021-07 0.354 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/28/2020 7 NDC:75594-021-06 208 L in 1 DRUM; Type 0: Not a Combination Product 07/28/2020 8 NDC:75594-021-08 1249 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product 07/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/28/2020 Labeler - Commercial Beverage Concepts, LLC (080925174) Establishment Name Address ID/FEI Business Operations Commercial Beverage Concepts, LLC 080925174 label(75594-021) , pack(75594-021) , relabel(75594-021) , repack(75594-021)