Label: MENTHOL CAMPHOR COUGH SUPPRESSANT TOPICAL ANALGESIC RUB (camphor- natural and menthol, unspecified form ointment
- NDC Code(s): 72342-220-04
- Packager: J.R. Watkins, LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 8, 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
- Uses
-
Warnings
For external use only. Avoid contact with eyes.
Ask a doctor before use if you have
- cough that occurs with too much phlegm (mucus)
- chronic cough that lasts such as occurs with smoking, asthma, or emphysema
When using this product, do not
- heat
- microwave
- add to hot water or any container where heating water. May cause splattering and result in burns.
-
Directions
Adults and children 2 years and older:
For cough
- rub on the throat and chest in a thick layer
- cover with a warm, dry cloth if desired
- clothing should be loose about throat and chest to help vapors reach the nose and mouth
- use up to three times daily or as directed by a doctor
For muscle aches and pain
- apply to affected area not more than 3 to 4 times daily
- children under 2 years of age: do not use
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 116 g Jar Box
-
INGREDIENTS AND APPEARANCE
MENTHOL CAMPHOR COUGH SUPPRESSANT TOPICAL ANALGESIC RUB
camphor (natural) and menthol, unspecified form ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72342-220 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 5.3 g in 100 g MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 2.8 g in 100 g Inactive Ingredients Ingredient Name Strength PARAFFIN (UNII: I9O0E3H2ZE) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72342-220-04 1 in 1 BOX 08/01/2023 1 116 g in 1 JAR; 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 08/01/2023 Labeler - J.R. Watkins, LLC. (081071049)