Label: 3D ANTISEPTIC HAND SANITIZER- isopropyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 80286-924-01, 80286-924-34 - Packager: 3d International Llc
- 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 4, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
Flammable, keep away from fire/flame
For external use only
Do not use
- in children less than 2 months of age
- on open skin wounds
When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72hours
- Directions
- Other information
- Inactive ingredients
- Questions?
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SPL UNCLASSIFIED SECTION
ALL PURPOSE
ORGANIC
WITH ALOE VERA HAND SOFTNER
TSA APPROVED SIZE
MADE IN USA
Manufactured by: 3D International, LLC.
20724 Centre Pointe Parkway,Unit 1
Santa Clarita, CA 91350FRESH SCENTED
CALIFORNIA PROPOSITION
PROP 65
FORMULATED IN ACCORDANCE WITH CDC RECOMMENDATIONS
Does not contain triclosan, benzalkonium chloride, or phthalates
FOR EMERGENCY CALLCHEMTREC (800) 424 9300
- Packaging
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INGREDIENTS AND APPEARANCE
3D ANTISEPTIC HAND SANITIZER
isopropyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80286-924 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80286-924-34 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/28/2020 2 NDC:80286-924-01 3790 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/28/2020 Labeler - 3d International Llc (044018501) Establishment Name Address ID/FEI Business Operations 3d International Llc 044018501 manufacture(80286-924)