Label: SOLGREAT ALCOHOL-FREE HAND SANITIZER- benzalkonium chloride gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 73913-004-01, 73913-004-02 - Packager: PANATURAL USA, INC.
- 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 April 22, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active lngredient
- Purpose
- Uses
-
Warnings
For external use only.Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears & mouth.
When using this product, avoid contact with eyes. In case of contact flush eyes with water.
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.
- Directions
- Inactive ingredients
- Keep out of reach of children
- Products Label-237mL SolGreat Alcohol-Free Hand Sanitizer
- Product Label- 500mL SolGreat Alcohol-Free Hand Sanitizer
-
INGREDIENTS AND APPEARANCE
SOLGREAT ALCOHOL-FREE HAND SANITIZER
benzalkonium chloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73913-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73913-004-01 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/27/2020 2 NDC:73913-004-02 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/23/2020 Labeler - PANATURAL USA, INC. (029572239)
