Label: OKGO DISINFECTANT- didecyl dimethyl ammonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 81476-101-01, 81476-101-02, 81476-101-03, 81476-101-04 - Packager: Henan Seagood Medical Equipment Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 25, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. 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. - 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
OKGO DISINFECTANT
didecyl dimethyl ammonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81476-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM CHLORIDE 0.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM (UNII: 7N6JUD5X6Y) (C10-C16)ALKYLDIMETHYLAMINE OXIDE (UNII: LF6BKC321J) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) DIOCTYLDIMONIUM CHLORIDE (UNII: 0X0RL40Y6H) WATER (UNII: 059QF0KO0R) METHYL BENZOATE (UNII: 6618K1VJ9T) TROLAMINE (UNII: 9O3K93S3TK) STEARALKONIUM CHLORIDE (UNII: 0OUO26BB88) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81476-101-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/26/2021 2 NDC:81476-101-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/26/2021 3 NDC:81476-101-03 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/26/2021 4 NDC:81476-101-04 450 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/26/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/26/2021 Labeler - Henan Seagood Medical Equipment Co., Ltd. (715343285) Establishment Name Address ID/FEI Business Operations Henan Seagood Medical Equipment Co., Ltd. 715343285 manufacture(81476-101)