Label: WILD WATERMELON- hand sanitizer spray
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Contains inactivated NDC Code(s)
NDC Code(s): 76150-284-51 - Packager: Bell International Laboratories, Inc
- 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 August 6, 2021
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- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
WILD WATERMELON
hand sanitizer sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76150-284 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LEMON OIL (UNII: I9GRO824LL) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERETH-26 (UNII: NNE56F2N14) ALOE VERA LEAF (UNII: ZY81Z83H0X) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) LIME OIL (UNII: UZH29XGA8G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76150-284-51 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/01/2021 Labeler - Bell International Laboratories, Inc (967781555)