Label: RELIEF HAND SANITIZING WIPES- ethanol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 79002-162-01, 79002-162-20 - Packager: Daehan P&H Co., Ltd.
- 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 June 22, 2020
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
- Uses
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
■ Remove the wipes one by one, and use on the skin gently.
■ There is a risk of contamination if the wet wipe is put back into
the packaging with unclean hands.
■ Do not throw away wipes in a flush toilet, as there is a risk of
clogging it.
■ Supervise children under 6 years of age when using.
■ Do not allow infants and toddlers swallow or put in the mouth.
■ Avoid direct inhalation of vapors during application.
(Headaches and irritation to mucous membranes may occur when
directly inhaled.)
■ Keep product in its original container as storing the product in
anything other than the original container may result in accidents
or cause the integrity of the product to diminish. - Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
RELIEF HAND SANITIZING WIPES
ethanol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79002-162 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79002-162-20 20 in 1 BOX 06/22/2020 1 NDC:79002-162-01 1 in 1 PACKET; 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 06/22/2020 Labeler - Daehan P&H Co., Ltd. (557818402) Establishment Name Address ID/FEI Business Operations Sauber Co.,Ltd. 690395844 manufacture(79002-162)