Label: CDC70HS HAND SANITIZER- ethanol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76984-442-01, 76984-442-02, 76984-442-03, 76984-442-04, view more76984-442-05, 76984-442-06, 76984-442-07 - Packager: Canadian Distribution Channel
- 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.
Drug Label Information
Updated August 10, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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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) (70%, 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
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WHEN USING
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
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel CDC70HS 100ml, 500ml, 1890ml, 2L and 3,79L, 300 ml, 60 ml
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INGREDIENTS AND APPEARANCE
CDC70HS HAND SANITIZER
ethanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76984-442 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL in 100 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76984-442-01 100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 2 NDC:76984-442-02 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 3 NDC:76984-442-03 1890 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 4 NDC:76984-442-04 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 5 NDC:76984-442-05 3790 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 6 NDC:76984-442-06 300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 7 NDC:76984-442-07 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/24/2020 Labeler - Canadian Distribution Channel (242043508) Registrant - Canadian Distribution Channel (242043508) Establishment Name Address ID/FEI Business Operations Canadian Distribution Channel 242043508 manufacture(76984-442)