Label: DISINFECTING WIPES cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 79683-005-01, 79683-005-02, 79683-005-03 - Packager: Hefei Inridy Medical Products 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 April 16, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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Warnings
For external use only
*When using this product do not use in or near the eyes
In case of contact, rinse eyes thoroughly with water*Stop use and ask a doctor if irritation or rash appears and lasts 72
hours
*Keep out of the reach of children.If swallowed, get medical help or
contact a Poison Control Center right away.
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DISINFECTING WIPES
disinfecting wipes clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79683-005 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 DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM CHLORIDE 0.2 g in 100 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PROPYLENE GLYCOL DIBUTYRATE (UNII: KQ2A0DW803) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79683-005-01 60 in 1 BAG; Type 0: Not a Combination Product 03/30/2020 2 NDC:79683-005-02 90 in 1 DRUM; Type 0: Not a Combination Product 03/30/2020 3 NDC:79683-005-03 160 in 1 DRUM; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Hefei Inridy Medical Products Co., Ltd (406390933) Establishment Name Address ID/FEI Business Operations Hefei Inridy Medical Products Co., Ltd 406390933 manufacture(79683-005)