Label: ELYPTOL LIGHT SCENT- ANTIMICROBIAL HAND GEL- ethanol gel
-
NDC Code(s):
69343-421-01,
69343-421-02,
69343-421-08,
69343-421-15, view more69343-421-16, 69343-421-32, 69343-421-42
- Packager: ELYPTOL 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 December 19, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient:
- Purpose
- Keep out reach of children
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
ELYPTOL LIGHT SCENT- ANTIMICROBIAL HAND GEL
ethanol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69343-421 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 7 mL in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) EUCALYPTOL (UNII: RV6J6604TK) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) PIROCTONE OLAMINE (UNII: A4V5C6R9FB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69343-421-02 1 in 1 CARTON 06/01/2016 1 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69343-421-08 1 in 1 CARTON 06/01/2016 2 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:69343-421-16 1 in 1 CARTON 06/01/2016 3 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:69343-421-32 1 in 1 CARTON 06/01/2016 4 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:69343-421-01 1 in 1 CARTON 01/13/2017 5 2 mL in 1 PACKET; Type 0: Not a Combination Product 6 NDC:69343-421-15 1 in 1 CARTON 01/13/2017 6 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:69343-421-42 1 in 1 CARTON 06/01/2016 7 1242 mL in 1 BOTTLE, DISPENSING; 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 part333A 06/01/2016 Labeler - ELYPTOL INC. (079594781)