Label: HAND SANITIZER FREE AND CLEAR- 62% ethyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 69366-314-05 - Packager: The Honest Company
- Category: HUMAN OTC DRUG LABEL
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 January 25, 2021
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- Official Label (Printer Friendly)
- Active ingredient
- Uses
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Warnings
For external use only
Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104 oF/40 oC
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin
Stop use and ask a doctor if irritation and redness devleop and persist for more than 72 hours
- Directions
- Inactive ingredients
- 8 oz label
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INGREDIENTS AND APPEARANCE
HAND SANITIZER FREE AND CLEAR
62% ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69366-314 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) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CHAMOMILE (UNII: FGL3685T2X) GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69366-314-05 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/31/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/31/2017 Labeler - The Honest Company (969962757)