Label: BONSCENT HAND SANITIZER BASIC- alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 73981-010-01, 73981-010-02, 73981-010-03 - Packager: Microbiome9 Life Science
- 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 27, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- INACTIVE INGREDIENT
- Purpose
-
Warnings
Warnings:
For external use only: hands
Flammable, Keep away from fire or flame.
When using this product ■ keep out of eyes. In case of contact with eyes, flush thoroughly with water ■ avoid contact with broken skin. ■ do not inhale or ingest.
Stop use and ask a doctor if ■ irritation and redness develop ■ condition persists for more than 72 hours
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other information
- PACKAGE LABEL - BONSCENT HAND SANITIZER BASIC GEL / 50ea carton
- PACKAGE LABEL - BONSCENT HAND SANITIZER BASIC GEL / 100ea carton
-
INGREDIENTS AND APPEARANCE
BONSCENT HAND SANITIZER BASIC
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73981-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 1.86 g in 3 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) Butylene Glycol (UNII: 3XUS85K0RA) Hexylene Glycol (UNII: KEH0A3F75J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73981-010-02 50 in 1 CARTON 03/01/2020 1 NDC:73981-010-01 3 mL in 1 PACKET; Type 0: Not a Combination Product 2 NDC:73981-010-03 100 in 1 CARTON 03/01/2020 2 NDC:73981-010-01 3 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/01/2020 Labeler - Microbiome9 Life Science (695631807) Registrant - Microbiome9 Life Science (695631807) Establishment Name Address ID/FEI Business Operations DongbangCosmetics Co., ltd. 694452564 manufacture(73981-010)