Label: PAIN CREAM- analgesic cream
- NDC Code(s): 79804-260-02
- Packager: Eagle Labs Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 15, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Uses:
- WARNINGS:
- WHEN USING THIS PRODUCT
- Stop Usage immediately and as a doctor if:
- If pregnant or breast-feeding:
- Keep out of reach of children
- Directions:
- Other Information
-
Inactive Ingredients:
Bis-Vinyl Dimethicone/Dimthicone Copolymer, C13-C14 Isoparaffin, Caprylic/Capric Triglyceride, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycol Stearate, Jojoba Oil, Laureth-7, Lavender Oil, Phenoxyethanol, Polyarylamide, Shea Butter, Simethicone, Sodium Acrylate/Sodium Acrylol Dimethyl Taurate Copolymer, Spearmint Oil, Water.
- INSTA EAZE: RUB THE PAIN AWAY
-
INGREDIENTS AND APPEARANCE
PAIN CREAM
analgesic creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79804-260 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.06 g in 1 g CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.05 g in 1 g Inactive Ingredients Ingredient Name Strength CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q) CAPRYLIC/CAPRIC ACID (UNII: DI775RT244) WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) PHENOXYETHANOL (UNII: HIE492ZZ3T) SHEA BUTTER (UNII: K49155WL9Y) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) LAURETH-7 (UNII: Z95S6G8201) LAVENDER OIL (UNII: ZBP1YXW0H8) SPEARMINT OIL (UNII: C3M81465G5) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCOL STEARATE (UNII: 0324G66D0E) JOJOBA OIL (UNII: 724GKU717M) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79804-260-02 59 g in 1 PACKAGE; Type 0: Not a Combination Product 08/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/22/2022 Labeler - Eagle Labs Inc. (118496872) Registrant - Eagle Labs Inc (118496872) Establishment Name Address ID/FEI Business Operations Eagle Labs Inc 118496872 manufacture(79804-260) , pack(79804-260) , label(79804-260)