Label: ALCOHOL FOAMING HAND SANITIZER- alcohol soap
- NDC Code(s): 62428-701-03, 62428-701-29, 62428-701-53, 62428-701-57
- Packager: Lawson Prodcuts, 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 March 14, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
-
Warnings
For external use only. Do not ingest.
FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition.
Avoid contact with eyes. In case of eye contact, flush with large quantities of water, seek medical attention if irritation persists.
If skin irritation develops, discontinue use. If irritation persists for more than 72 hours, seek medical attention.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away. - Inactive Ingredients
- Purpose
- Alcohol Foaming Hand Sanitizer
- Directions
- Uses
- Alcohol Foaming Hand Sanitizer
-
INGREDIENTS AND APPEARANCE
ALCOHOL FOAMING HAND SANITIZER
alcohol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62428-701 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 mL in 1 mL Inactive Ingredients Ingredient Name Strength D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP) WATER (UNII: 059QF0KO0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) Product Characteristics Color blue Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62428-701-03 750 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2019 2 NDC:62428-701-57 550 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2019 3 NDC:62428-701-53 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2019 4 NDC:62428-701-29 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/14/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/14/2019 Labeler - Lawson Prodcuts, Inc (005438890) Registrant - Betco Corporation, Ltd (005050158) Establishment Name Address ID/FEI Business Operations Betco Corporation, Ltd 005050158 manufacture(62428-701)