ProCure Anti Itch

Product NDC
55681-038
11-digit product format
556810038
Labeler code
55681
Product ID
55681-038_3afe387c-ef43-215d-e063-6394a90a41b5
Type
HUMAN OTC DRUG
Nonproprietary name
Camphor 0.5%
Dosage form
LOTION
Route
TOPICAL
Labeler
Twin Med LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-09-15
Substance
CAMPHOR (NATURAL)
Active strength
.5 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ProCure Anti Itch
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAMPHOR (NATURAL).5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiN20HL7Q941
Rxcui2059052

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55681-038-75ProCure Anti Itch222 mL in 1 BOTTLE, PUMPLOTION2221

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2059052camphor 0.5 % Topical LotionPSN3afe387c-ef42-215d-e063-6394a90a41b51
2059052camphor 5 MG/ML Topical LotionSCD3afe387c-ef42-215d-e063-6394a90a41b51
2059052camphor 0.5 % Topical LotionSY3afe387c-ef42-215d-e063-6394a90a41b51

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
55681-038-7555681003875222 mL in 1 BOTTLE, PUMP (55681-038-75) 222 ml2025-09-15NoNoCurrent