Label: SURFS UP BATH CO. HAND SANITIZER- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 90050-001-01, 90050-001-02, 90050-001-03, 90050-001-04 - Packager: The Little Bath Co. 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 July 18, 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
- Use
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Warnings
For external use only.
Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104°F/40°C.
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 develop and persist for more than 72 hours.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
SURFS UP BATH CO. HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:90050-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 67 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS) (UNII: CH428W5O62) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) GLYCERIN (UNII: PDC6A3C0OX) FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:90050-001-01 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/09/2020 2 NDC:90050-001-02 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/09/2020 3 NDC:90050-001-03 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/09/2020 4 NDC:90050-001-04 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/09/2020 Labeler - The Little Bath Co. LLC (079120294)