Label: 75% ALCOHOL DISINFECTANT liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 75132-002-01, 75132-002-02, 75132-002-03, 75132-002-04, view more75132-002-05, 75132-002-06, 75132-002-07, 75132-002-08, 75132-002-09, 75132-002-10 - Packager: Guangdong Kemei Pharmaceutical Technology 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 June 3, 2020
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
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
75% ALCOHOL DISINFECTANT
75% alcohol disinfectant liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75132-002 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75132-002-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 2 NDC:75132-002-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 3 NDC:75132-002-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 4 NDC:75132-002-04 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 5 NDC:75132-002-05 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 6 NDC:75132-002-06 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 7 NDC:75132-002-07 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 8 NDC:75132-002-08 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 9 NDC:75132-002-09 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 10 NDC:75132-002-10 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/12/2020 Labeler - Guangdong Kemei Pharmaceutical Technology Co., Ltd. (554528507) Registrant - Guangdong Kemei Pharmaceutical Technology Co., Ltd. (554528507) Establishment Name Address ID/FEI Business Operations Guangdong Kemei Pharmaceutical Technology Co., Ltd. 554528507 manufacture(75132-002)
