Neutrogena Sun Rescue After Sun Medicated Relief 4.5 mg/g
CAMPHOR (SYNTHETIC) · GEL · Kenvue Brands LLC
Neutrogena Sun Rescue After Sun Medicated Relief is a gel containing camphor (synthetic) at 4.5 mg/g, taken topical. Manufactured by Kenvue Brands LLC.
Key Facts
- Brand Name
- Neutrogena Sun Rescue After Sun Medicated Relief
- Generic Name
- CAMPHOR (SYNTHETIC)
- NDC Code (Product)
69968-0721- Manufacturer
- Kenvue Brands LLC
- Strength
- 4.5 mg/g
- Dosage Form
- GEL
- Route
- TOPICAL
- Marketing Status
- Application #
- M017
- Marketing Start
- 10/01/2021
Recall History
No Recall HistoryFull Prescribing Information
Indications & Usage
Use temporarily relieves pain and itching associated with sunburn
Dosage & Administration
Directions adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: ask a doctor
Warnings
Warnings For external use only. Flammable: Keep away from fire or flame When using this product avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.
Frequently Asked Questions
What is Neutrogena Sun Rescue After Sun Medicated Relief used for?
Neutrogena Sun Rescue After Sun Medicated Relief contains CAMPHOR (SYNTHETIC). It is a gel taken topical. Consult your doctor for specific uses.
Is Neutrogena Sun Rescue After Sun Medicated Relief a controlled substance?
Neutrogena Sun Rescue After Sun Medicated Relief is not classified as a controlled substance by the DEA.
What is the generic name for Neutrogena Sun Rescue After Sun Medicated Relief?
The generic name for Neutrogena Sun Rescue After Sun Medicated Relief is CAMPHOR (SYNTHETIC). There are 12 other brand versions of CAMPHOR (SYNTHETIC).
What is the NDC code for Neutrogena Sun Rescue After Sun Medicated Relief 4.5 mg/g?
The NDC (National Drug Code) for Neutrogena Sun Rescue After Sun Medicated Relief 4.5 mg/g is 69968-0721, listed by Kenvue Brands LLC.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)