Label: ANTIMICROBIAL ALCOHOL HAND WIPES- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 44019-003-00 - Packager: Yinjing Medical Technology (Shanghai) 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 December 27, 2017
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- Official Label (Printer Friendly)
- Antimicrobial Alcohol Gel Hand wipes
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- To start feed: Remove cover and discard seal from container, From center of toweled roll , pull up wipe corner; tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover.Pull through about one inch. Replace cover,Pull out wipes as needed and snap off at 90°angle. Keep cap closed to prevent moisture loss.
- Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry.
- If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, Sanitize with a second wipe.
- Discard after single use.
- To start feed: Remove cover and discard seal from container, From center of toweled roll , pull up wipe corner; tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover.Pull through about one inch. Replace cover,Pull out wipes as needed and snap off at 90°angle. Keep cap closed to prevent moisture loss.
- Other information
- Inactive ingredients
- Antimicrobial Alcohol Gel Hand Wipes
- PRINCIPAL DISPLAY PANEL
- Antimicrobial Alcohol Gel Hand wipes 135 Wipes (44019-003-00)
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INGREDIENTS AND APPEARANCE
ANTIMICROBIAL ALCOHOL HAND WIPES
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44019-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 65.9 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44019-003-00 135 in 1 CANISTER 08/03/2016 1 3.42 g 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 part333E 08/03/2016 Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535) Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)