Label: CARELAND PAIN RELIEF PLUS- camphor, menthol, methyl salicylate patch
- NDC Code(s): 75568-039-01
- Packager: Planet (Anhui) Pharmaceutical Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Use
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Warnings
For external use only
Do not use
- More than one patch on your body at a time
- On cut, irritated or swollen skin
- On puncture wounds
- For more than one week without consulting a doctor
- If you are allergic to any active or inactive ingredients
- If pouch is damaged or opened
When using this product
- Use only as directed
- Read all follow all directions and warnings
- Do not allow contact with the eyes
- do not allow contact with the eyes
- Do not use at the same time as other topical anesthetics
- Do not bandage tightly or apply local heat (such as heating pads) to the area of use
- Do not microwave
- Dispose of used patch in manner that always keeps product away from children and pets, Used patches still contain the drug product that can produce serious adverse effects is a child or pet chews or ingests this patch.
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Directons
Adults and children 12 years of age and over:
- Clean and dry affected area
- Carefully remove backing from patch
- Apply sticky side of patch to affected area
- Use one patch for up to 8 hours
- Discard patch after single use
- Apply 1 patch at a time to affected area, not more than 3 to 4 times daily
Children under 12 years of age: consult a physician.
- Other information
- Inactive ingredients
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
CARELAND PAIN RELIEF PLUS
camphor, menthol, methyl salicylate patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75568-039 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 31 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 60 mg in 1 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 100 mg in 1 g Inactive Ingredients Ingredient Name Strength PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) MINERAL OIL (UNII: T5L8T28FGP) TERPENE RESIN (UNII: GR35AH6YDN) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75568-039-01 1 in 1 BOX 08/02/2025 1 56 in 1 BAG 1 0.7 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/02/2025 Labeler - Planet (Anhui) Pharmaceutical Co., Ltd. (618456104) Registrant - Planet (Anhui) Pharmaceutical Co., Ltd. (618456104) Establishment Name Address ID/FEI Business Operations Planet (Anhui) Pharmaceutical Co., Ltd. 618456104 manufacture(75568-039)

