Label: 100% PURE HAND SANITIZER- ethyl alcohol spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 52667-010-01 - Packager: Purity Cosmetics
- 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 March 20, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings:
- STORAGE AND HANDLING
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- OTHER SAFETY INFORMATION
- STOP USE
- Directions:
- Other Ingredients:
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
100% PURE HAND SANITIZER
ethyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52667-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) TEA TREE OIL (UNII: VIF565UC2G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52667-010-01 50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/22/2020 Labeler - Purity Cosmetics (055795259) Registrant - Our Babylon LLC (105266218) Establishment Name Address ID/FEI Business Operations Our Babylon LLC 105266218 manufacture(52667-010)