Label: U.S. LEGAL SUPPORT HAND SANITIZER- ethyl alcohol gel
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NDC Code(s):
73788-107-01,
73788-107-02,
73788-107-03,
73788-107-04, view more73788-107-05, 73788-107-06, 73788-107-07, 73788-107-08
- Packager: Hangzhou Huiji 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 February 24, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- 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 & mouth.
When using this product, avoid contact with eyes.
In case of contact, flush eyes with water.
Stop use and ask a doctor if redness or irritation
develop and persist for more than 72 hours.
Keep out of reach of children. Children must be
supervised in use of this product. - Directions
- Other Information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
U.S. LEGAL SUPPORT HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73788-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) CARBOMER 934 (UNII: Z135WT9208) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73788-107-01 200 in 1 CARTON 08/12/2020 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:73788-107-02 150 in 1 CARTON 08/12/2020 2 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:73788-107-03 100 in 1 CARTON 08/12/2020 3 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:73788-107-04 24 in 1 CARTON 08/12/2020 4 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:73788-107-05 20 in 1 CARTON 08/12/2020 5 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:73788-107-06 6 in 1 CARTON 08/12/2020 6 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:73788-107-07 4 in 1 CARTON 08/12/2020 7 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 8 NDC:73788-107-08 4 in 1 CARTON 08/12/2020 8 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/12/2020 Labeler - Hangzhou Huiji Biotechnology Co., Ltd. (526893497) Establishment Name Address ID/FEI Business Operations Hangzhou Huiji Biotechnology Co., Ltd. 526893497 manufacture(73788-107)