Label: VICKS VAPO RUB- camphor, mentol, eucalyptus oil ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 73097-015-01, 73097-015-24 - Packager: Savings Distributors LLC
- This is a repackaged label.
- Source NDC Code(s): 37000-544
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 August 1, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
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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)
• persistent or chronic cough 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.Stop use and ask a doctor if
• muscle aches and pains worsen or persist for more than 7 days or
clear up and occur again within a few days.
• cough persists for more than 1 week, tends to recur, or isaccompanied by fever, rash, or persistent headache. A persistent
cough may be a sign of a serious condition.
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Directions
see important warnings under “When using this product”
• adults and children 2 years and over:
• for cough suppression
• rub a thick layer on throat & chest
• cover with a warm, dry cloth if desired
• keep clothing loose about throat and chest to help vapors reach thenose and mouth
• use up to three times daily or as directed by doctor
• for muscle / joint minor aches and pains apply to affected area notmore than 3 to 4 times daily
• children under 2 years: do not use - Other information
- Inactive ingredients
- Questions or comments?
- Package Label
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INGREDIENTS AND APPEARANCE
VICKS VAPO RUB
camphor, mentol, eucalyptus oil ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73097-015(NDC:37000-544) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.048 g in 1 g EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 0.012 g in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.026 g in 1 g Inactive Ingredients Ingredient Name Strength CEDAR LEAF OIL (UNII: BJ169U4NLG) NUTMEG OIL (UNII: Z1CLM48948) PETROLATUM (UNII: 4T6H12BN9U) THYMOL (UNII: 3J50XA376E) TURPENTINE OIL (UNII: C5H0QJ6V7F) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73097-015-24 24 in 1 CARTON 07/22/2019 1 12 g in 1 CONTAINER; Type 0: Not a Combination Product 2 NDC:73097-015-01 12 g in 1 CONTAINER; Type 0: Not a Combination Product 07/22/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 07/22/2019 Labeler - Savings Distributors LLC (010527359) Establishment Name Address ID/FEI Business Operations Savings Distributors LLC 010527359 repack(73097-015)
