Label: MD SELECTIONS HAND SANITIZER- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79416-555-01 - Packager: Dermapeutics
- Category: HUMAN OTC DRUG LABEL
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 July 6, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- USE
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Warnings
- Do not use in the eyes. In case of contact rinse thoroughly with water
- Do not use on children less than 2 months of age.
- For external use only.
- Flammable, keep away from heat and flame.
- Stop use and ask doctor if
- Irritation and redness develop and persist for more than 72hrs
- Swallowed, get medical attention or contact poison control center right away.
- Directions:
- Other Information:
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
MADE WITHOUT
- PARABENS
- TRICLOSAN
- BENZALKONIUM CHLORIDE
*A portion of the proceeds will go to support
KILLS 99.99% OF GERMS
T A P S®
TRAGEDY ASSISTANCE PROGRAM FOR SURVIVORS
NO ANIMAL TESTING
Made in the USA
Distributed By:
Dermapeutics Corp
Calabasas, CA 91302
Caring for the families of America's fallen heros since 1994.
TAPS Mission Statement:
TAPS provides comfort, care and resources to all those grieving the death of a military loved one, Since 1994, TAPS has provided comfort and hope 24/7 through a national peer support network and connection to grief resources, all at no cost to surviving families and loved ones.
TAPS.org
WWW.DERMAPEUTICS.COM
- Packaging
-
INGREDIENTS AND APPEARANCE
MD SELECTIONS HAND SANITIZER
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79416-555 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H) ORANGE OIL (UNII: AKN3KSD11B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79416-555-01 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/07/2020 Labeler - Dermapeutics (859082237)