Label: WM BROWN X ACQUA DI GABRIEL- hand sanitizing mist lmp spray
ACQUA DI GABRIAL- hand sanitizing mist lc spray
ACQUA DI GABRIAL- hand sanitizing mist herbal spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 79930-7106-1, 79930-7106-4, 79930-7107-1, 79930-7107-4, view more79930-7110-1 - Packager: Nexderma
- 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 October 19, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Inactive ingredients
- Use
- KEEP OUT OF REACH OF CHILDREN
-
Warnings
Keep away form fire and flame.
Flammable
For external use on hands only.
Keep out of eye, ears and mouth.
If contact in eyes, flush thoroughly with water.
Keep out of reach of children.
If swallowed seek medical help immediately or call your poison control center.
Store between 15-30 (58-86F)
Avoid freezing and excessive heat above 40C (104F)
Will damage wood finishes, plastics and some fabrics. - Do not use
- Directions
- Purpose
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
WM BROWN X ACQUA DI GABRIEL
hand sanitizing mist lmp sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79930-7110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) 0.03 mL in 100 mL SILVER (UNII: 3M4G523W1G) 0.5 mL in 100 mL WATER (UNII: 059QF0KO0R) POMEGRANATE SEED OIL (UNII: 0UI45XV0T6) LEMON OIL (UNII: I9GRO824LL) MANDARIN OIL (UNII: NJO720F72R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79930-7110-1 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/30/2020 ACQUA DI GABRIAL
hand sanitizing mist lc sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79930-7107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) 0.03 mL in 100 mL SILVER (UNII: 3M4G523W1G) 0.5 mL in 100 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79930-7107-1 125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/30/2020 2 NDC:79930-7107-4 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/30/2020 ACQUA DI GABRIAL
hand sanitizing mist herbal sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79930-7106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) 0.03 mL in 100 mL SILVER (UNII: 3M4G523W1G) 0.5 mL in 100 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79930-7106-1 125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/30/2020 2 NDC:79930-7106-4 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/30/2020 Labeler - Nexderma (079533940) Establishment Name Address ID/FEI Business Operations Nexderma 079533940 manufacture(79930-7106, 79930-7107, 79930-7110) , pack(79930-7106, 79930-7107, 79930-7110) , label(79930-7106, 79930-7107, 79930-7110)