Label: HAND SANITIZER GEL- alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 75722-005-01, 75722-005-02 - Packager: Rapid Cure Technologies INC
- 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 31, 2020
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- Directions
- Other information
- Inactive ingredients
- DESCRIPTION
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER GEL
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75722-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) HEPTANAL (UNII: 92N104S3HF) ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75722-005-02 946.3 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/31/2020 2 NDC:75722-005-01 3785 mL in 1 JUG; Type 0: Not a Combination Product 07/31/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/31/2020 Labeler - Rapid Cure Technologies INC (017489374)