Label: PRICILL 70% ETOH HAND MIST SWEET PLEASURE- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76882-0001-1 - Packager: BIO-FD&C. Co., Ltd.
- 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 April 29, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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PRINCIPAL DISPLAY PANEL
Water, Butyric Acid, Porphyra 334, Rosa Damascena Callus Culture Extract, Lactobacillus Ferment Filtrate, Artemisia Princeps Extract, Linalool, Limonene, Butylene Glycol, Hexyl Cinnamal, 1,2 Hexanediol, Alpha Isomethyl Ionone, Hydroxycitronellal, Citronellol, Geraniol, Fragrance
.• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears
and lasts.
• Keep Out of Reach of Children.
• Do not eat.
• If swallowed, get medical help or contact a Poison Control
Center right away -
INGREDIENTS AND APPEARANCE
PRICILL 70% ETOH HAND MIST SWEET PLEASURE
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76882-0001 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 BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BUTYRIC ACID (UNII: 40UIR9Q29H) WATER (UNII: 059QF0KO0R) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76882-0001-1 100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/01/2020 Labeler - BIO-FD&C. Co., Ltd. (688203268) Registrant - BIO-FD&C. Co., Ltd. (688203268) Establishment Name Address ID/FEI Business Operations BIO-FD&C. Co., Ltd. 688203268 manufacture(76882-0001)