Active Ingredient
Camphor, USP 11%
The following Structured Product Label (SPL) was submitted to the FDA by Dlc Laboratories, Inc. for the product De La Cruz Camphor (NDC 24286-1521). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, stop use and consult a doctor if, if pregnant or breastfeeding,, keep out of the reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Camphor, USP 11%
External analgesic
for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains
For external use only
avoid contact with eyes or mucous membranes
do not apply to wounds or damaged skin
do not bandage tightly or use with a heating pad
condition worsens or if symptoms persist for more than 7 days
symptoms clear up and occur again within a few days.
excessive skin irritation develops
consult a doctor before use.
If swallowed, get medical help or contact a Poison Control Center right away.
adults and children 2 years of age or older, apply to affected area not more than 3 to 4 times daily
children under 2 years of age: consult a doctor
polyethylene glycol
1-800-858-3889 or www.dlclabs.com
De La Cruz
CAMPHOR
Ointment 11%
Pain relieving rub
2.5 OZ (70.9g)
FAST, PENETRATING RELIEF FOR:
Muscle and joint pain
Backaches and arthritis
Strains and sprains
Itching
NON-IRRITATING
WATER WASHABLE
NO PARABENS OR ARTIFICIAL FRAGRANCES OR COLORS
Manufactured by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA
Questions: 1-800-858-3889
www.dlclabs.com (c) DLC
* Please review the disclaimer below.