Label: HAND GEL gel
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Contains inactivated NDC Code(s)
NDC Code(s): 79867-002-01, 79867-002-02, 79867-002-03 - Packager: Guangzhou meizi biotechnology 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 March 30, 2022
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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Warnings
For external use only. Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears or mouth.
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Stop use or ask for a doctor if redness or irritation develops and persists for more than 72 hours.
Keep out of reach of children. Children must be supervised in use of this product.
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND GEL
hand gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79867-002 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 CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79867-002-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 2 NDC:79867-002-02 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 3 NDC:79867-002-03 30 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 - Guangzhou meizi biotechnology co. LTD (403308233) Establishment Name Address ID/FEI Business Operations Guangzhou meizi biotechnology co. LTD 403308233 manufacture(79867-002)