NDC | 72130-003-01, 72130-003-02, 72130-003-03 |
Set ID | ecfa5e4a-ed70-4f32-87ea-0e60c8dac3d0 |
Category | HUMAN OTC DRUG LABEL |
Packager | Registered Chemicals Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SANISMART 3
ethanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72130-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) PANTHENOL (UNII: WV9CM0O67Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72130-003-01 1250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/01/2018 2 NDC:72130-003-02 1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/01/2018 3 NDC:72130-003-03 3750 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/01/2018 Labeler - Registered Chemicals Corporation (046652831)