Label: ANMEIKANG DISINFECTANT WIPES- disinfectant wipes cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 81496-002-01, 81496-002-02, 81496-002-03, 81496-002-04, view more81496-002-05, 81496-002-06, 81496-002-07, 81496-002-08, 81496-002-09, 81496-002-10, 81496-002-11, 81496-002-12, 81496-002-13 - Packager: Liaoning MeiXin Pharmaceutical Company
- 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 March 26, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only.
When using this product avoid to contact eyes, mouth, wounds and other sensitive parts. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
The product is insoluble in water, do not dispose the used wet wipes into flush toilets.
The product is disposable, for single use, please do not reuse.
- Directions
- Other Information
- KEEP OUT OF REACH OF CHILDREN
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
ANMEIKANG DISINFECTANT WIPES
disinfectant wipes clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81496-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g Inactive Ingredients Ingredient Name Strength PHENOXYETHANOL (UNII: HIE492ZZ3T) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) WATER (UNII: 059QF0KO0R) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81496-002-01 10 in 1 BAG 03/01/2021 1 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 2 NDC:81496-002-02 20 in 1 BAG 03/01/2021 2 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 3 NDC:81496-002-03 30 in 1 BAG 03/01/2021 3 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 4 NDC:81496-002-04 40 in 1 BAG 03/01/2021 4 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 5 NDC:81496-002-05 50 in 1 BAG 03/01/2021 5 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 6 NDC:81496-002-06 60 in 1 BAG 03/01/2021 6 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 7 NDC:81496-002-07 80 in 1 BAG 03/01/2021 7 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 8 NDC:81496-002-08 20 in 1 BOX 03/01/2021 8 0.00764 g in 1 POUCH; Type 0: Not a Combination Product 9 NDC:81496-002-09 30 in 1 BOX 03/01/2021 9 0.00764 g in 1 POUCH; Type 0: Not a Combination Product 10 NDC:81496-002-10 50 in 1 BOX 03/01/2021 10 0.00764 g in 1 POUCH; Type 0: Not a Combination Product 11 NDC:81496-002-11 60 in 1 CANISTER 03/01/2021 11 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 12 NDC:81496-002-12 100 in 1 CANISTER 03/01/2021 12 0.00764 g in 1 PATCH; Type 0: Not a Combination Product 13 NDC:81496-002-13 120 in 1 CANISTER 03/01/2021 13 0.00764 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 part333A 03/01/2021 Labeler - Liaoning MeiXin Pharmaceutical Company (712964681) Registrant - Liaoning MeiXin Pharmaceutical Company (712964681) Establishment Name Address ID/FEI Business Operations Liaoning MeiXin Pharmaceutical Company 712964681 manufacture(81496-002)