Label: DALIS HAND SANITIZER- alcohol solution
-
Contains inactivated NDC Code(s)
NDC Code(s): 77639-001-01, 77639-001-02, 77639-001-03, 77639-001-04, view more77639-001-05, 77639-001-06, 77639-001-07, 77639-001-08, 77639-001-09, 77639-001-10, 77639-001-11, 77639-001-12, 77639-001-13, 77639-001-14, 77639-001-15, 77639-001-16, 77639-001-17, 77639-001-18, 77639-001-19, 77639-001-20, 77639-001-21, 77639-001-22, 77639-001-23, 77639-001-24, 77639-001-25, 77639-001-26, 77639-001-27, 77639-001-28 - Packager: Zhejiang Yongjin 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 May 12, 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
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DALIS HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77639-001 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 GLYCEROL FORMAL (UNII: 3L7GR2604E) WATER (UNII: 059QF0KO0R) ALOE (UNII: V5VD430YW9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77639-001-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 2 NDC:77639-001-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 3 NDC:77639-001-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 4 NDC:77639-001-04 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 5 NDC:77639-001-05 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 6 NDC:77639-001-06 150 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 7 NDC:77639-001-07 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 8 NDC:77639-001-08 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 9 NDC:77639-001-09 280 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 10 NDC:77639-001-10 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 11 NDC:77639-001-11 350 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 12 NDC:77639-001-12 380 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 13 NDC:77639-001-13 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 14 NDC:77639-001-14 450 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 15 NDC:77639-001-15 480 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 16 NDC:77639-001-16 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 17 NDC:77639-001-17 600 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 18 NDC:77639-001-18 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 19 NDC:77639-001-19 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 20 NDC:77639-001-20 2500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 21 NDC:77639-001-21 3800 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 22 NDC:77639-001-22 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 23 NDC:77639-001-23 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 24 NDC:77639-001-24 20000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 25 NDC:77639-001-25 25000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 26 NDC:77639-001-26 50000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 27 NDC:77639-001-27 120000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 28 NDC:77639-001-28 1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/12/2020 Labeler - Zhejiang Yongjin Biotechnology Co., Ltd (542189693) Establishment Name Address ID/FEI Business Operations Zhejiang Yongjin Biotechnology Co., Ltd 542189693 manufacture(77639-001)
