Label: NANO SILVER CLEANSER HAND SANITIZER- silver cation,alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79702-302-01, 79702-302-02, 79702-302-03, 79702-302-04, view more79702-302-05, 79702-302-06 - Packager: DDUnion, Co.,Ltd
- 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 August 22, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- USE
- WHEN USING
- Warnings
- Do not use
- Stop use and ask doctor
- PURPOSE
- Keep out of reach of children
- Direction
- Other information
- Inactive ingredients
- label
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INGREDIENTS AND APPEARANCE
NANO SILVER CLEANSER HAND SANITIZER
silver cation,alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79702-302 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION 0.0025 g in 100 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.05 mL in 100 mL Inactive Ingredients Ingredient Name Strength LEMON OIL (UNII: I9GRO824LL) WATER (UNII: 059QF0KO0R) POLYSORBATE 20 (UNII: 7T1F30V5YH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79702-302-01 50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/11/2020 2 NDC:79702-302-02 70 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/11/2020 3 NDC:79702-302-03 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/11/2020 4 NDC:79702-302-04 200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/11/2020 5 NDC:79702-302-05 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/11/2020 6 NDC:79702-302-06 1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/11/2020 Labeler - DDUnion, Co.,Ltd (694100331) Registrant - DDUnion, Co.,Ltd (694100331) Establishment Name Address ID/FEI Business Operations DDUnion, Co.,Ltd 694100331 manufacture(79702-302)