Label: ALCOHOL WIPES cloth
-
Contains inactivated NDC Code(s)
NDC Code(s): 74658-013-01, 74658-013-02, 74658-013-03, 74658-013-04, view more74658-013-05, 74658-013-06, 74658-013-07, 74658-013-08, 74658-013-09 - Packager: GUANGZHOU XUELEI COSMETIC 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 November 10, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES
-
WARNINGS
FOR EXTERNAL USE ONLY.
FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.
AVOID CONTACT WITH EYES, IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER IMMEDIATELY.
KEEP OUT OF REACH OF CHILDREN EXCEPT UNDER ADULT SUPERVISION.
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
IF IRRITATION DEVELOPS, DISCONTINUE USE AND CONSULT A DOCTOR.
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ALCOHOL WIPES
alcohol wipes clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74658-013 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 TERT-BUTYL ALCOHOL (UNII: MD83SFE959) WATER (UNII: 059QF0KO0R) DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74658-013-01 1 in 1 BAG 10/10/2020 1 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 2 NDC:74658-013-02 75 in 1 BOTTLE 10/10/2020 2 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 3 NDC:74658-013-03 80 in 1 BOTTLE 10/10/2020 3 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 4 NDC:74658-013-04 100 in 1 BOTTLE 10/10/2020 4 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 5 NDC:74658-013-05 120 in 1 BOTTLE 10/10/2020 5 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 6 NDC:74658-013-06 130 in 1 BOTTLE 10/10/2020 6 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 7 NDC:74658-013-07 150 in 1 BOTTLE 10/10/2020 7 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 8 NDC:74658-013-08 180 in 1 BOTTLE 10/10/2020 8 4.3 mL in 1 PATCH; Type 0: Not a Combination Product 9 NDC:74658-013-09 200 in 1 BOTTLE 10/10/2020 9 4.3 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 10/10/2020 Labeler - GUANGZHOU XUELEI COSMETIC CO.,LTD. (526885026) Registrant - GUANGZHOU XUELEI COSMETIC CO.,LTD. (526885026) Establishment Name Address ID/FEI Business Operations GUANGZHOU XUELEI COSMETIC CO.,LTD. 526885026 manufacture(74658-013) , label(74658-013) , pack(74658-013)