Label: SHOPKO CAMPHOR PHENOL GEL- camphor, phenol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 37012-734-04 - Packager: Shopko
- 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 July 29, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Keep Out of Reach of Children
- Uses
-
Warnings
For external use only.
Do not use over large areas of the body or with a bandage. Ask a doctor before use if you have a deep puncture wound, animal bites, or serious burns.
When using this product: do not use near the eyes. If contact occurs, rinse eyes thoroughly with water and obtain medical attention.
Stop use and consult a doctor if: conditions worsen or symptoms persist more than 7 days, or clears up and returns again in a few days.
- Directions
- Inactive Ingredients
- Package/Label Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SHOPKO CAMPHOR PHENOL GEL
camphor, phenol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37012-734 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 10.8 mg in 1 g PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL 4.7 mg in 1 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP) 77.75 mg in 1 g SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 5.75 mg in 1 g GLYCERIN (UNII: PDC6A3C0OX) 0.5 mg in 1 g EUCALYPTUS OIL (UNII: 2R04ONI662) 0.500 mg in 1 g Product Characteristics Color YELLOW Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37012-734-04 1 g in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 03/15/2013 Labeler - Shopko (023252638) Registrant - Shopko (023252638) Establishment Name Address ID/FEI Business Operations OraLabs 801824756 MANUFACTURE(37012-734) , LABEL(37012-734)