Label: DAISY CLEAN SANITIZER- hypochlorous acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 75696-0008-1, 75696-0008-2, 75696-0008-3, 75696-0008-4 - Packager: JD corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 6, 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
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Warning
For external use only
When using this product
• if followmg abnormal symptoms persist, discontinue use
Irritation around the eyes. ears, mucous membranes.
including the mouth.under the skin irritation and rashes
• Stop immediately and consult a doctor if you experience
1) Hypersensitivity symptoms such as erythema,
itching and dermatitis.
2) Skin Irritation
3) Following Instructions when using medication
(1) For external use only (Do not use internally)
(2) Avoid gelling into the eyes (if contact occurs,
wash well with clean water)
• Be careful not to inhale or use excessively for a long time
(ingesting ethanol repeatedly causes irritation to mucous
membranes and headaches or other symptoms may appear.
When used repeatedly in the same area, skin irritation may occur.
• Do not use the product for a tong time in the same area as
swelling, inflammation or sickness may occur due to absorption
through the skin. It is not recommended using this one area
that have been medically treated with a cast or bandage.
• Do not use in combination with soap or antibacterial
cleansing agents. - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredient
- Product label
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INGREDIENTS AND APPEARANCE
DAISY CLEAN SANITIZER
hypochlorous acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75696-0008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 0.005 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75696-0008-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/06/2021 2 NDC:75696-0008-2 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/06/2021 3 NDC:75696-0008-3 4000 mL in 1 CONTAINER; Type 0: Not a Combination Product 10/06/2021 4 NDC:75696-0008-4 20000 mL in 1 CONTAINER; Type 0: Not a Combination Product 10/06/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/06/2021 Labeler - JD corporation (694848434) Registrant - JD corporation (694848434) Establishment Name Address ID/FEI Business Operations JD corporation 694848434 manufacture(75696-0008)