Label: DEFENSE AG DISINFECTANT- ea disinfectant spray spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79930-7116-4, 79930-7116-5, 79930-7116-6 - Packager: Nexderma
- 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 November 4, 2020
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Inactive ingredients
- Use
- KEEP OUT OF REACH OF CHILDREN
- Warnings
- Do not use
- Directions
- Purpose
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DEFENSE AG DISINFECTANT
ea disinfectant spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79930-7116 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 0.125 mL in 100 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength SILVER (UNII: 3M4G523W1G) 0.2 mL in 100 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79930-7116-4 473 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/09/2020 2 NDC:79930-7116-6 946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/09/2020 3 NDC:79930-7116-5 3790 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/09/2020 Labeler - Nexderma (079533940) Establishment Name Address ID/FEI Business Operations Nexderma 079533940 manufacture(79930-7116) , pack(79930-7116) , label(79930-7116)