Label: BONITA ALCOHOL SANITIZING- alcohol sanitizing spray spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 78409-001-01, 78409-001-02, 78409-001-03, 78409-001-04, view more78409-001-05, 78409-001-06, 78409-001-07, 78409-001-08, 78409-001-09, 78409-001-10, 78409-001-11, 78409-001-12, 78409-001-13, 78409-001-14 - Packager: Moreno and Sons Company
- 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 4, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients:
- Purpose
- Uses:
- Warning:
- KEEP OUT OF REACH OF CHILDREN
- Directions：
- Other information:
- Inactive Ingredients:
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
- Package Label
-
INGREDIENTS AND APPEARANCE
BONITA ALCOHOL SANITIZING
alcohol sanitizing spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78409-001 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 WATER (UNII: 059QF0KO0R) 25 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78409-001-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 2 NDC:78409-001-02 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 3 NDC:78409-001-03 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 4 NDC:78409-001-04 150 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 5 NDC:78409-001-05 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 6 NDC:78409-001-06 235 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 7 NDC:78409-001-07 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 8 NDC:78409-001-08 260 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 9 NDC:78409-001-09 290 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 10 NDC:78409-001-10 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 11 NDC:78409-001-11 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 12 NDC:78409-001-12 950 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 13 NDC:78409-001-13 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 14 NDC:78409-001-14 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/20/2020 Labeler - Moreno and Sons Company (060555980) Registrant - GUANGZHOU XUELEI COSMETIC CO.,LTD. (526885026) Establishment Name Address ID/FEI Business Operations GUANGZHOU XUELEI COSMETIC CO.,LTD. 526885026 pack(78409-001) , manufacture(78409-001) , label(78409-001)
