Label: BITE AND STING RELIEF WELL AT WALGREENS- benzocaine - 5.00% spray
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-3190-03 - Packager: Walgreens
- 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 January 30, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient Purpose
- PURPOSE
- Uses
- WarningsFor external use only
- When using this product
- Stop use and ask a doctor if
- KEEP OUT OF REACH OF CHILDREN
- Direction
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Inactive ingredients
Aloe Barbadensis Leaf Juice, Ascorbic Acid, Camphor, Chamomilla Recutita (Matricaria) Flower Extract, Cholecalciferol, Diisopropyl Adipate,
Eugenia Caryophyllus (Clove) Flower Oil, Fragrance, Mentha Piperita (Peppermint) Oil, Octyldodecanol, Olea Europaea (Olive) Fruit Oil,
PEG-8 Dimethicone, Propylene Glycol, Pyridoxine HCl, Retinyl Palmitate, SD Alcohol 40, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica,
Tocopheryl Acetate, Zea Mays (Corn) Oil - Questions and comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BITE AND STING RELIEF WELL AT WALGREENS
benzocaine - 5.00% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-3190 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 5 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ASCORBIC ACID (UNII: PQ6CK8PD0R) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) CHAMOMILE (UNII: FGL3685T2X) Cholecalciferol (UNII: 1C6V77QF41) Diisopropyl Adipate (UNII: P7E6YFV72X) CLOVE OIL (UNII: 578389D6D0) PEPPERMINT OIL (UNII: AV092KU4JH) Octyldodecanol (UNII: 461N1O614Y) OLIVE OIL (UNII: 6UYK2W1W1E) PEG-8 Dimethicone (UNII: GIA7T764OD) Propylene Glycol (UNII: 6DC9Q167V3) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) Alcohol (UNII: 3K9958V90M) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Sodium Propoxyhydroxypropyl Thiosulfate Silica (UNII: 208G222332) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CORN OIL (UNII: 8470G57WFM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-3190-03 85 g in 1 CAN; Type 0: Not a Combination Product 03/15/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 03/15/2013 Labeler - Walgreens (008965063) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(0363-3190) , label(0363-3190)