Label: HAND SANITIZER- ethyl alcohol gel
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NDC Code(s):
51414-912-01,
51414-912-02,
51414-912-03,
51414-912-04, view more51414-912-05, 51414-912-06, 51414-912-07, 51414-912-08, 51414-912-09, 51414-912-10, 51414-912-11, 51414-912-12, 51414-912-13, 51414-912-14, 51414-912-15, 51414-912-16, 51414-912-17, 51414-912-18, 51414-912-19
- Packager: Yuyao Jessie Commodity Co., Ltd.
- 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 March 18, 2022
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51414-912 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51414-912-01 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 2 NDC:51414-912-02 10 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 3 NDC:51414-912-03 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 4 NDC:51414-912-04 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 5 NDC:51414-912-05 480 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 6 NDC:51414-912-06 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 7 NDC:51414-912-07 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 8 NDC:51414-912-08 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 9 NDC:51414-912-09 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 10 NDC:51414-912-10 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 11 NDC:51414-912-11 90 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 12 NDC:51414-912-12 8 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 13 NDC:51414-912-13 0.9 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 14 NDC:51414-912-14 5 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 15 NDC:51414-912-15 25 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 16 NDC:51414-912-16 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 17 NDC:51414-912-17 35 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 18 NDC:51414-912-18 75 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 19 NDC:51414-912-19 18 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/10/2020 Labeler - Yuyao Jessie Commodity Co., Ltd. (529892305) Registrant - Yuyao Jessie Commodity Co., Ltd. (529892305) Establishment Name Address ID/FEI Business Operations Yuyao Jessie Commodity Co., Ltd. 529892305 manufacture(51414-912)