Label: CHIGGEREX- benzocaine cream
- NDC Code(s): 52412-350-17, 52412-350-50
- Packager: RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
For external use only.
When using this product
- avoid contact with the eyes
Stop use and ask a doctor if
- condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- INSTRUCTIONS FOR USE
-
INACTIVE INGREDIENT
Aloe Barbadensis Leaf Juice, Ascorbic Acid, Camphor, Chamomilla Recutita (Matricaria) Flower Extract, Cholecalciferol, Diazolidinyl Urea, Disodium EDTA, Eugenia Caryophyllus (Clove) Flower Oil, Fragrance,Mentha Piperita (Peppermint) Oil, Methylparaben, Octyldodecanol, Olea Europaea (Olive) Fruit Extract, PEG-2 Stearate, PEG-2 Stearate SE, PEG-8 Dimethicone, Propylene Glycol, Propylparaben, Pyridoxine HCl, Retinyl Palmitate, Sodium Propoxyhydroxypropyl Thiosulfate Silica, Tocopheryl Acetate, Water, Zea Mays (Corn) Oil
- SPL UNCLASSIFIED SECTION
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CHIGGEREX
benzocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52412-350 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 0.1 g in 1 g Inactive Ingredients Ingredient Name Strength SILICA (UNII: ETJ7Z6XBU4) ASCORBIC ACID (UNII: PQ6CK8PD0R) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X) PEG-8 DIMETHICONE (UNII: GIA7T764OD) RETINYL PALMITATE (UNII: 1D1K0N0VVC) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PYRIDOXINE HCL (UNII: 68Y4CF58BV) CHAMOMILE (UNII: FGL3685T2X) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) OCTYLDODECANOL (UNII: 461N1O614Y) CAMPHOR, (-)- (UNII: 213N3S8275) ZEA MAYS (CORN) OIL (UNII: 8470G57WFM) METHYLPARABEN (UNII: A2I8C7HI9T) EUGENIA CARYOPHYLLUS (CLOVE) FLOWER OIL (UNII: 578389D6D0) MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH) PEG-2 STEARATE (UNII: 94YQ11Y95F) SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332) WATER (UNII: 059QF0KO0R) CHOLECALCIFEROL (UNII: 1C6V77QF41) OLEA EUROPAEA (OLIVE) FRUIT (UNII: 2M6QWV94OC) PROPYLPARABEN (UNII: Z8IX2SC1OH) Product Characteristics Color yellow (Off-White to Yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52412-350-50 50 g in 1 JAR; Type 0: Not a Combination Product 02/01/2020 2 NDC:52412-350-17 170 g in 1 JAR; Type 0: Not a Combination Product 02/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/01/2020 Labeler - RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH (061995007)
