Label: HAN-SAN TOPICAL 80 liquid
HAN-SAN GEL gel
HAN-SAN TOPICAL liquid
HAN-SAN GEL WITH ALOE- alcohol gel
SOBER-SAN liquid
-
NDC Code(s):
73943-945-01,
73943-945-02,
73943-945-03,
73943-945-04, view more73943-945-05, 73943-945-06, 73943-945-07, 73943-945-08, 73943-945-09, 73943-945-10, 73943-945-11, 73943-946-01, 73943-946-02, 73943-946-03, 73943-946-04, 73943-946-05, 73943-946-06, 73943-947-01, 73943-947-02, 73943-947-03, 73943-949-01, 73943-949-02, 73943-949-03, 73943-949-04, 73943-949-05, 73943-949-06, 73943-949-07, 73943-952-01, 73943-952-02, 73943-952-03, 73943-952-04, 73943-952-05, 73943-952-06
- Packager: Rite-Kem Incorporated
- 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 March 15, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
Han-San Gel 70% alcohol
Fast Acting Effective
Kills 99.9% of Germs and Bacteria on Hands
Made in USA
WWW.RITE-KEM.COM
Sold By
Rite-Kem, Inc.
703 Westmoreland Drive
Tupelo, MS 38801
662-840-6060
NDC: 73943-945-xx
****************************
Han-San Topical 70% alcohol
Alcohol Antiseptic 70%
Topical Solution Hand sanitizer
Non-Sterile Solution
FDA registered
Kills 99.9% of Germs and Bacteria on Hands
Made in USA
WWW.RITE-KEM.COM
Sold By
Rite-Kem, Inc.
703 Westmoreland Drive
Tupelo, MS 38801
662-840-6060
NDC: 73943-946-xx
*******************
Han-San Topical 80% alcohol
Alcohol Antiseptic 80%
Topical Solution Hand sanitizer
Non-Sterile Solution
FDA registered
Kills 99.9% of Germs and Bacteria on Hands
Made in USA
WWW.RITE-KEM.COM
Sold By
Rite-Kem, Inc.
703 Westmoreland Drive
Tupelo, MS 38801
662-840-6060
NDC: 73943-947-xx
*************************
Han-San Gel with Aloe 70% alcohol
Fast Acting Effective
Kills 99.99% of Germs and bacterial on Hands
Made in USA
WWW.RITE-KEM.COM
Sold By
Rite-Kem, Inc.
703 Westmoreland Drive
Tupelo, MS 38801
662-840-6060
NDC: 73943-949-xx
-
INGREDIENTS AND APPEARANCE
HAN-SAN TOPICAL 80Â
han-san topical 80 liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73943-947 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL  in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  HYDROGEN PEROXIDE (UNII: BBX060AN9V)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73943-947-01 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 12/06/2021 2 NDC:73943-947-02 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 12/06/2021 3 NDC:73943-947-03 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/24/2020 HAN-SAN GELÂ
han-san gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73943-945 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  TROLAMINE (UNII: 9O3K93S3TK)  GLYCERIN (UNII: PDC6A3C0OX)  LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  ETHYL ACRYLATE (UNII: 71E6178C9T)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73943-945-01 59.14 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 2 NDC:73943-945-02 1123.79 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 3 NDC:73943-945-03 3785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 4 NDC:73943-945-04 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 5 NDC:73943-945-05 208198 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 6 NDC:73943-945-06 1040990 mL in 1 TANK; Type 0: Not a Combination Product 03/24/2020 7 NDC:73943-945-07 118.29 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/18/2020 8 NDC:73943-945-08 354.9 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 9 NDC:73943-945-09 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 10 NDC:73943-945-10 44 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 11 NDC:73943-945-11 592 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/24/2020 HAN-SAN TOPICALÂ
han-san topical liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73943-946 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX)  HYDROGEN PEROXIDE (UNII: BBX060AN9V)  LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73943-946-01 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 2 NDC:73943-946-02 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 3 NDC:73943-946-03 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 4 NDC:73943-946-04 208198 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 5 NDC:73943-946-05 1040990 mL in 1 TANK; Type 0: Not a Combination Product 03/24/2020 6 NDC:73943-946-06 18927 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/24/2020 HAN-SAN GEL WITH ALOEÂ
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73943-949 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73943-949-01 59.14 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2021 2 NDC:73943-949-02 118.29 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2021 3 NDC:73943-949-03 354.88 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2021 4 NDC:73943-949-04 591.47 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2021 5 NDC:73943-949-05 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2021 6 NDC:73943-949-06 3785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2021 7 NDC:73943-949-07 208198 mL in 1 DRUM; Type 0: Not a Combination Product 03/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/15/2021 SOBER-SANÂ
sober-san liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73943-952 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C16) (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C16) 0.1 g  in 100 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73943-952-01 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 2 NDC:73943-952-02 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 3 NDC:73943-952-03 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 4 NDC:73943-952-04 208198 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 5 NDC:73943-952-05 1040990 mL in 1 TANK; Type 0: Not a Combination Product 03/24/2020 6 NDC:73943-952-06 18927 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/15/2020 Labeler - Rite-Kem Incorporated (786892927) Establishment Name Address ID/FEI Business Operations Rite-Kem Incorporated 786892927 manufacture(73943-945, 73943-946, 73943-947, 73943-949, 73943-952)