Label: NANO PURE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71530-024-01, 71530-024-02, 71530-024-03, 71530-024-04, view more71530-024-05 - Packager: Nano Global
- 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 December 13, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive Ingredients
- Questions?
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Principal Display Panel
nano™ PURE
Active Skin Protection
Patented Formula
Kills 99.99% of Germs
24 HOUR GERM BARRIER
Join the Nano™ movement and register today at MYNANO.COM
Long-Lasting
Most hand sanitizers only protect for seconds
Safe*
Nano Pure™ forms a safe germ barrier
*when used as directed
Protects
Kills 99.99% of germs
Be Well, Do Good
Your purchase supports the fight against infectious diseases worldwide
Dermatologist Tested
U.S. Pat. No. 6,613,755
Manufactured for
Nano Global Corp. Austin, TX 78701
MADE IN THE U.S.A.
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INGREDIENTS AND APPEARANCE
NANO PURE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71530-024 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength 1-OCTADECANAMINIUM, N,N-DIMETHYL-N-(3-(TRIHYDROXYSILYL)PROPYL) CHLORIDE (UNII: GLJ50K866T) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71530-024-01 10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/26/2017 2 NDC:71530-024-02 47.32 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/26/2017 3 NDC:71530-024-03 236.59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/26/2017 4 NDC:71530-024-04 800 mL in 1 BAG; Type 0: Not a Combination Product 06/26/2017 5 NDC:71530-024-05 207 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/29/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/26/2017 Labeler - Nano Global (079594740)