Label: BLESS YOU- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73708-919-84 - Packager: CarrollClean LLC
- 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 August 25, 2020
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- Official Label (Printer Friendly)
- Active Ingredients
- Uses
- WARNINGS
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- Keep out of reach of children.
- When Using this product
- Label
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INGREDIENTS AND APPEARANCE
BLESS YOU
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73708-919 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) 0.8843 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.1431 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.0093 mL in 100 mL WATER (UNII: 059QF0KO0R) 36.0815 mL in 100 mL ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) 0.1051 mL in 100 mL PHENOXYETHANOL (UNII: HIE492ZZ3T) 0.0404 mL in 100 mL DIISOPROPYLAMINE (UNII: BR9JLI40NO) 0.2724 mL in 100 mL CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) 0.3906 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73708-919-84 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/24/2020 Labeler - CarrollClean LLC (081222623) Establishment Name Address ID/FEI Business Operations CarrollClean LLC 081222623 manufacture(73708-919)