Label: EUCALYPTUS HAND WIPES- isopropyl alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 74110-002-01, 74110-002-02 - Packager: Dr. Brite
- 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 16, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- PURPOSE
- Inactive ingredients
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DOSAGE & ADMINISTRATION
Directions For Use
Open the lid and peel back the seal. When finished, close to retain moisture.
Remove a wipe, wipe thoroughly until clean. Larger messes may require two wipes.
Allow to air dry. No rinsing or drying is required, even on food prep areas.
NOT SUITABLE FOR: Porous materials, leather, silk clothing or stained woods.
- Storage & Disposal
- Caution
- First-Aid
- For Questions or Concerns
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
EUCALYPTUS HAND WIPES
isopropyl alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74110-002 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 EUCALYPTUS PIPERITA LEAF OIL (UNII: 3V7YF916NL) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) PEPPERMINT OIL (UNII: AV092KU4JH) LAURIC ACID (UNII: 1160N9NU9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74110-002-01 54 in 1 BAG 02/16/2022 1 5.4 mL in 1 PATCH; Type 0: Not a Combination Product 2 NDC:74110-002-02 10 in 1 POUCH 02/16/2022 2 5.4 mL in 1 PATCH; 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 02/16/2022 Labeler - Dr. Brite (079902543) Establishment Name Address ID/FEI Business Operations Dr. Brite 079902543 manufacture(74110-002) , label(74110-002) , pack(74110-002) , analysis(74110-002)