Label: MAGIC FOR PAIN RELIEF- camphor, methyl salicylate, menthol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 71419-001-01 - Packager: Zhuhai Aofute Medical Technology Co, Ltd
- 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 December 7, 2020
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Directions
- Warnings
- When Using This Product
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Stop Use and Ask a Doctor If
Condition worsens
Symptoms persist for more than 7 days
Symptoms clear up and occur again within a few days
Excessive irritation of the skin develops
Nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs
When using for pain of arthritis: pain persists for more than 10 days, redness is present, in conditions affecting children 12 years of age.
- Keep Out of Reach of Children
- Other Information
- Inactive Ingredients
- Manufactured by Zhuhai Aofute Medical Technology Co., Ltd86-756-6832001 Monday - Friday 8:30 - 5:30
- Drug Facts
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INGREDIENTS AND APPEARANCE
MAGIC FOR PAIN RELIEF
camphor, methyl salicylate, menthol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71419-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 10 g in 100 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 30 g in 100 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 16 g in 100 mL Inactive Ingredients Ingredient Name Strength CARTHAMUS TINCTORIUS WHOLE (UNII: 5EMV416J82) CAPSICUM ANNUUM WHOLE (UNII: 7FKZ3QQQ1F) PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U) REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ) DAEMONOROPS DRACO WHOLE (UNII: 1C8HA8O22C) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) MUSCONE (UNII: UPS3C6CV36) BORNEOL (UNII: M89NIB437X) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71419-001-01 1 in 1 BOX 12/01/2011 1 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/01/2011 Labeler - Zhuhai Aofute Medical Technology Co, Ltd (544472634)