Label: QUICK-DRYING HAND SANITIZER- hand sanitizer liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 75244-001-01, 75244-001-02, 75244-001-03 - Packager: Shandong Kehong 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.
Drug Label Information
Updated April 14, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
- Packaging Labels - Main Display Panel
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INGREDIENTS AND APPEARANCE
QUICK-DRYING HAND SANITIZER
hand sanitizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75244-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 1.1 g in 100 g ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75244-001-01 100 g in 1 BOTTLE; Type 0: Not a Combination Product 04/14/2020 2 NDC:75244-001-02 500 g in 1 BOTTLE; Type 0: Not a Combination Product 04/14/2020 3 NDC:75244-001-03 1000 g in 1 BOTTLE; Type 0: Not a Combination Product 04/14/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/14/2020 Labeler - Shandong Kehong Medical Technology Co.,Ltd. (554527496) Establishment Name Address ID/FEI Business Operations Shandong Kehong Medical Technology Co.,Ltd 554527496 manufacture(75244-001)