Label: LEMYN ORGANICS MEDICAL GRADE HAND SANITIZER GEL- hand sanitizer gel
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Contains inactivated NDC Code(s)
NDC Code(s): 67923-101-02, 67923-101-08, 67923-101-12 - Packager: Vege Labs LLC.
- 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 7, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Uses
- Warnings
- Directions
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Inactive Ingredients
JOJOBA OIL (UNII: 724GKU717M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ORANGE OIL (UNII: AKN3KSD11B)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
COMFREY ROOT (UNII: M9VVZ08EKQ)
SUNFLOWER OIL (UNII: 3W1JG795YI)
PANTHENOL (UNII: WV9CM0O67Z)
AVOCADO OIL (UNII: 6VNO72PFC1)
WATER (UNII: 059QF0KO0R)
- Other Information
- Questions and Comments?
- Dosage and Administration
- Indications and Usage
- 2 fl oz Label
- COMPANY INFORMATION
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INGREDIENTS AND APPEARANCE
LEMYN ORGANICS MEDICAL GRADE HAND SANITIZER GEL
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67923-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) 0.001 mL in 100 mL JOJOBA OIL (UNII: 724GKU717M) 0.001 mL in 100 mL AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) 0.04275 mL in 100 mL WATER (UNII: 059QF0KO0R) 28.28725 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 1.0075 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.0025 mL in 100 mL SUNFLOWER OIL (UNII: 3W1JG795YI) 0.001 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.001 mL in 100 mL CARBOMER 940 (UNII: 4Q93RCW27E) 0.33 mL in 100 mL ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B) 0.3 mL in 100 mL AVOCADO OIL (UNII: 6VNO72PFC1) 0.001 mL in 100 mL PANTHENOL (UNII: WV9CM0O67Z) 0.025 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67923-101-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/28/2020 2 NDC:67923-101-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/28/2020 3 NDC:67923-101-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/28/2020 Labeler - Vege Labs LLC. (117878620) Establishment Name Address ID/FEI Business Operations Vege Labs LLC. 117878620 manufacture(67923-101)