Label: ALCOHOL WIPES cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 74835-012-01, 74835-012-02, 74835-012-03, 74835-012-04 - Packager: Hangzhou Lookon Commodity 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 October 18, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings:
For external use only
Flammable: Keep away from flame or high heat.
When use this product avoid contact with the eyes,face and broken skin.
Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.
Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- STORAGE AND HANDLING
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALCOHOL WIPES
alcohol wipes clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74835-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74835-012-01 250 in 1 PAIL 08/03/2022 1 0.68 mL in 1 PATCH; Type 0: Not a Combination Product 2 NDC:74835-012-02 1000 in 1 PAIL 08/03/2022 2 0.68 mL in 1 PATCH; Type 0: Not a Combination Product 3 NDC:74835-012-03 1200 in 1 BAG 08/03/2022 3 0.68 mL in 1 PATCH; Type 0: Not a Combination Product 4 NDC:74835-012-04 50 in 1 BAG 08/03/2022 4 0.68 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 08/03/2022 Labeler - Hangzhou Lookon Commodity Co., Ltd. (541760483) Registrant - Hangzhou Lookon Commodity Co., Ltd. (541760483) Establishment Name Address ID/FEI Business Operations Hangzhou Lookon Commodity Co., Ltd. 541760483 manufacture(74835-012)