Label: WET WIPES- ethyl alcohol swab
-
Contains inactivated NDC Code(s)
NDC Code(s): 69821-003-01, 69821-003-02, 69821-003-03, 69821-003-04, view more69821-003-05, 69821-003-06, 69821-003-07, 69821-003-08, 69821-003-09, 69821-003-10, 69821-003-11 - Packager: Zhejiang Qimei 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 November 2, 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
- Uses
-
Warnings
. FOR EXTERNAL USE ONLY
. FLAMMABL E, KEEP AWAY FROM FIRE OR FL AME
●When using this product avoid contact with eyes. In case of eye contact,
flush eyes with water and seek medical help.
●If swallowed drink large amounts of water and seek medical attention.
●Avoid contact with face and broken skin. If contact occurs, flush with water.
●Stop use and ask a doctor if rritation or redness develops
Note Do not store above00°F. Non-stainingMay discolor some fabrics. - Keep out of reach of children
- Directions
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WET WIPES
ethyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69821-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69821-003-01 10 in 1 PACKAGE 04/20/2020 1 2.5 g in 1 POUCH; Type 0: Not a Combination Product 2 NDC:69821-003-02 20 in 1 PACKAGE 04/20/2020 2 2.5 g in 1 POUCH; Type 0: Not a Combination Product 3 NDC:69821-003-03 30 in 1 PACKAGE 04/20/2020 3 2.5 g in 1 POUCH; Type 0: Not a Combination Product 4 NDC:69821-003-04 50 in 1 PACKAGE 04/20/2020 4 2.5 g in 1 POUCH; Type 0: Not a Combination Product 5 NDC:69821-003-05 80 in 1 PACKAGE 04/20/2020 5 2.5 g in 1 POUCH; Type 0: Not a Combination Product 6 NDC:69821-003-06 100 in 1 BAG 04/20/2020 6 2.5 g in 1 POUCH; Type 0: Not a Combination Product 7 NDC:69821-003-07 160 in 1 BAG 04/20/2020 7 0.48 g in 1 POUCH; Type 0: Not a Combination Product 8 NDC:69821-003-09 135 in 1 PAIL 04/20/2020 8 0.48 g in 1 POUCH; Type 0: Not a Combination Product 9 NDC:69821-003-08 1200 in 1 BAG 04/20/2020 9 0.47 g in 1 POUCH; Type 0: Not a Combination Product 10 NDC:69821-003-10 250 in 1 PAIL 04/20/2020 10 0.48 g in 1 POUCH; Type 0: Not a Combination Product 11 NDC:69821-003-11 1500 in 1 PAIL 04/20/2020 11 0.48 g in 1 POUCH; 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 04/20/2020 Labeler - Zhejiang Qimei Commodity Co.,Ltd. (544331136) Registrant - Zhejiang Qimei Commodity Co.,Ltd. (544331136) Establishment Name Address ID/FEI Business Operations Zhejiang Qimei Commodity Co.,Ltd. 544331136 manufacture(69821-003)
