Label: DARANJO- benzalkonium chloride solution
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Contains inactivated NDC Code(s)
NDC Code(s): 78084-003-01, 78084-003-02, 78084-003-03, 78084-003-04 - Packager: Matilde Gómez López
- 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 September 7, 2020
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
- 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
DARANJO
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78084-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 g in 1000 mL Inactive Ingredients Ingredient Name Strength SODIUM NITRITE (UNII: M0KG633D4F) 0.3 g in 1000 mL ALCOHOL (UNII: 3K9958V90M) 4 mL in 1000 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78084-003-01 65 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/07/2020 2 NDC:78084-003-02 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/07/2020 3 NDC:78084-003-03 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/07/2020 4 NDC:78084-003-04 330 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/07/2020 Labeler - Matilde Gómez López (951577135) Registrant - Matilde Gómez López (951577135) Establishment Name Address ID/FEI Business Operations Matilde Gómez López 951577135 manufacture(78084-003) , pack(78084-003) , label(78084-003)