Label: HAND SANITIZER- hand soap gel
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Contains inactivated NDC Code(s)
NDC Code(s): 55029-002-01, 55029-002-02 - Packager: Shenzhen Derun'en Science & Technology Development 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 November 21, 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
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Directions
- Put proper amount of the hand sanitizer into your palm and gently rub it over your palms, the back of your hands, fingers and the spaces between your fingers. Rub your hands together continuously until they are dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
hand soap gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55029-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 1 mg in 100 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55029-002-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 2 NDC:55029-002-02 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Shenzhen Derun'en Science & Technology Development Co., Ltd (550292933) Registrant - Shenzhen Derun'en Science & Technology Development Co., Ltd (550292933) Establishment Name Address ID/FEI Business Operations Shenzhen Derun'en Science & Technology Development Co., Ltd 550292933 manufacture(55029-002) , label(55029-002)