Label: DEFENSE AG- defense ag sanitizing gel gel
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Contains inactivated NDC Code(s)
NDC Code(s): 79930-7102-1, 79930-7102-2, 79930-7102-3, 79930-7102-4 - Packager: Nexderma Inc
- 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 30, 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)
- INACTIVE INGREDIENT
- Use
- KEEP OUT OF REACH OF CHILDREN
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Warnings
Keep away from fire and flame.
Flammable
For external use on hands only
Keep out of eyes, ears and mouth.
If contact in eyes, flush thoroughly with water.
Keep out of reach of children
If swallowed seek medical help immediately or call poison control center
Store between 15-30C (58-86F)
Avoid freezing and excessive heat above 40C (104F)
Will damage wood finishes, plastics and some fabrics
- Do not use
- DOSAGE & ADMINISTRATION
- PURPOSE
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DEFENSE AG
defense ag sanitizing gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79930-7102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) 0.2 mL in 100 mL CURCUMIN (UNII: IT942ZTH98) 1.3 mL in 100 mL WATER (UNII: 059QF0KO0R) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79930-7102-1 100 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/30/2020 2 NDC:79930-7102-2 250 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/30/2020 3 NDC:79930-7102-4 500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/30/2020 4 NDC:79930-7102-3 350 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 09/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/30/2020 Labeler - Nexderma Inc (079533940) Establishment Name Address ID/FEI Business Operations Nexderma 079533940 manufacture(79930-7102) , pack(79930-7102) , label(79930-7102)