Label: UNIVERSAL SANITIZING POMEGRANATE AND CHERRY- ethyl alcohol aerosol, spray
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Contains inactivated NDC Code(s)
NDC Code(s): 52000-405-00 - Packager: Universal Distribution Center 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 February 8, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
• Extremely flammable aerosol, keep away from fire/flame.
• Keep away from heat, hot surfaces, open flames and other ignition sources.
• Pressurized container. Do not piece or burn even after use.
• Protect from sunlight.
• For external use only
Do not use
• on children less than 2 months of age
• on open skin wounds
When using this product • Avoid use on/or around eyes, mouth, broken/irritated skin or large areas of Body. In case of contact with eyes, rinse thoroughly with water several minutes. • do not inhale or ingest.
Stop and ask doctor if
• irritation persist
• or if product is swallowed
- Directions
- Other information
- Inactive ingredients
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SPL UNCLASSIFIED SECTION
Kills 99.9% Germs
2 in 1
Odor Eliminating & Kills Germs Quickly
Contains 75% Alcohol
KEEP OUT OF REACH OF CHILDREN.
Quick All Purpose Sanitizer
Eliminates Odor & Deodorizes the Air
Fights the Spread of Germs
Prevents Growth of Mold & Mildew
Sanitizes Hard & Soft Surfaces
Mfd for and Distributed By:
Universal Distribution Center LLC
96 Distribution Boulevard, Edison, NJ 08817
Made in Turkey
www.universaldc.com
www.universalbrandsusa.com
NO CFCs
CONTAINS NO CFCs WHICH DEPLETE THE OZONE LAYER
"U" is a Registered Trademark of Universal Distribution Center LLC.
- Packaging
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INGREDIENTS AND APPEARANCE
UNIVERSAL SANITIZING POMEGRANATE AND CHERRY
ethyl alcohol aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-405 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength BUTANE (UNII: 6LV4FOR43R) PROPANE (UNII: T75W9911L6) ISOBUTANE (UNII: BXR49TP611) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52000-405-00 550 mL in 1 CAN; Type 0: Not a Combination Product 02/07/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 02/07/2021 Labeler - Universal Distribution Center Llc (019180459)