Label: SIGNATURE CARE BITE AND STING RELIEF- benzocaine spray
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Contains inactivated NDC Code(s)
NDC Code(s): 21130-143-01 - Packager: Safeway
- 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 March 11, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients
Aloe Barbadensis Leaf Extract
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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SIGNATURE CARE BITE AND STING RELIEF
benzocaine sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-143 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 ASCORBIC ACID (UNII: PQ6CK8PD0R) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CLOVE OIL (UNII: 578389D6D0) PEPPERMINT OIL (UNII: AV092KU4JH) OLIVE OIL (UNII: 6UYK2W1W1E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CORN OIL (UNII: 8470G57WFM) ALOE VERA LEAF (UNII: ZY81Z83H0X) OCTYLDODECANOL (UNII: 461N1O614Y) PEG-8 DIMETHICONE (UNII: GIA7T764OD) CAMPHOR (NATURAL) (UNII: N20HL7Q941) CHOLECALCIFEROL (UNII: 1C6V77QF41) ALCOHOL (UNII: 3K9958V90M) CHAMOMILE (UNII: FGL3685T2X) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-143-01 85 g in 1 CAN; Type 0: Not a Combination Product 03/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 03/11/2020 Labeler - Safeway (009137209) Establishment Name Address ID/FEI Business Operations Inspec Solutions LLC 081030372 manufacture(21130-143)