Label: NO TOUCH APPLICATION CHEST RUB WELL AT WALGREENS- camphor 4.80% eucalyptus oil 1.20% menthol 2.60% stick
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-3267-02 - Packager: Walgreens
- 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 February 19, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredients Purpose
- PURPOSE
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Directions
See important warnings under "When using this product." Remove cap and twist up tube.
■ adults and children 2 years and over: ■ rub a thick layer on chest and throat or rub on sore aching muscles ■ cover loosely with a warm, dry cloth, if desired ■ keep clothing loose about throat/chest to help vapors reach the nose/mouth ■ repeat up to three times per 24 hours or as directed by doctor ■ children under 2 years do not use.
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WarningsFor external use only
Avoid contact with eyes.
Do not use ■ by mouth ■ with tight
bandages ■ in nostrils ■ on wounds or
damaged skin
Ask a doctor before you use if you have
■ a cough that occurs with too much
phlegm (mucus) ■ Persistent or chronic
cough such as occurs with smoking,
asthma or emphysema.
tWhen using this product, do not ■ heat
■ microwave ■ add to hot water or any
container where heating water may cause
spattering and result in burns.
Stop use and ask a doctor if ■ muscle
aches and pain persist for more than 7
days or come back ■ cough lasts more
than 7 days, comes back, or occurs with
fever, rash, or persistent headache - Keep out of reach of children.
- Uses
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NO TOUCH APPLICATION CHEST RUB WELL AT WALGREENS
camphor 4.80% eucalyptus oil 1.20% menthol 2.60% stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-3267 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 4.8 g in 100 g EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 1.2 g in 100 g Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) Menthol 2.6 g in 100 g Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) Mineral Oil (UNII: T5L8T28FGP) NUTMEG OIL (UNII: Z1CLM48948) Petrolatum (UNII: 4T6H12BN9U) Thymol (UNII: 3J50XA376E) CEDAR LEAF OIL (UNII: BJ169U4NLG) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Turpentine (UNII: XJ6RUH0O4G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-3267-02 43 g in 1 TUBE; Type 0: Not a Combination Product 09/15/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 09/15/2015 Labeler - Walgreens (008965063) Registrant - Product Quest Mfg. (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg. 927768135 manufacture(0363-3267) , label(0363-3267)
