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NDC 24286-1521-05 De La Cruz Camphor 11 g/100g Details

De La Cruz Camphor 11 g/100g

De La Cruz Camphor is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by DLC Laboratories, Inc.. The primary component is CAMPHOR (SYNTHETIC).

Product Information

NDC	24286-1521
Product ID	24286-1521_cdd0f519-3002-4130-90e0-9d9c430090bd
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	De La Cruz Camphor
Proprietary Name Suffix	n/a
Non-Proprietary Name	CAMPHOR
Product Type	HUMAN OTC DRUG
Dosage Form	OINTMENT
Route	TOPICAL
Active Ingredient Strength	11
Active Ingredient Units	g/100g
Substance Name	CAMPHOR (SYNTHETIC)
Labeler Name	DLC Laboratories, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2024-12-31

Package

Package Images

NDC 24286-1521-05 (24286152105)

Pricing Information	N/A
NDC Package Code	24286-1521-5
Billing NDC	24286152105
Package	155.9 g in 1 JAR (24286-1521-5)
Marketing Start Date	2021-03-10
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 62359237-de2d-4497-bfd6-36991cfc8acf Details

Active Ingredient

Camphor, USP 11%

Purpose

External analgesic

Uses

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains

Warnings

For external use only

When using this product

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

Stop use and consult a doctor if

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

If pregnant or breastfeeding,

consult a doctor before use.

KEEP OUT OF THE REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Inactive ingredient

polyethylene glycol

Questions?

1-800-858-3889 or www.dlclabs.com

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 70.9 g Jar Label

De La Cruz®

Clinically Tested*

CAMPHOR

OINTMENT 11%

Pain Relieving Rub

2.5 OZ (70.9 g)

Principal Display Panel - 70.9 g Jar Label

INGREDIENTS AND APPEARANCE

DE LA CRUZ CAMPHOR

camphor ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:24286-1521
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	11 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:24286-1521-2	70.9 g in 1 JAR; Type 0: Not a Combination Product	07/26/2012
2	NDC:24286-1521-5	155.9 g in 1 JAR; Type 0: Not a Combination Product	03/10/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	07/26/2012

Labeler - DLC Laboratories, Inc. (093351930)

Name	Address	ID/FEI	Business Operations
Establishment
DLC Laboratories, Inc.		093351930	MANUFACTURE(24286-1521) , LABEL(24286-1521)

Revised: 3/2021

Document Id: cdd0f519-3002-4130-90e0-9d9c430090bd

Set id: 62359237-de2d-4497-bfd6-36991cfc8acf

Version: 7

Effective Time: 20210323