Anti-Scar Drops

Product NDC: 63083-2084
Requested package NDC: 63083-2084-2
11-digit product format: 630832084
Labeler code: 63083
Product ID: 63083-2084_e82549c8-f10f-4e84-b444-e58e5eb195df
Type: HUMAN OTC DRUG
Nonproprietary name: Anti-Scar Drops
Dosage form: LIQUID
Route: ORAL
Labeler: Professional Complementary Health Formulas
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1984-08-15
Substance: ACONITUM NAPELLUS WHOLE; ALLYLTHIOUREA; ANHYDROUS DIBASIC CALCIUM PHOSPHATE; ARNICA MONTANA WHOLE; GRAPHITE; LACTOSE, X-RAY EXPOSED (1000 RAD); NITRIC ACID; POTASSIUM ALUM; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAF
Active strength: 6; 6; 6; 100; 12; 60; 8; 6; 6; 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 15 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

Additional Listing Data#

Finished product: Yes
Brand name base: Anti-Scar Drops
Brand name suffix: 2084
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
THUJA OCCIDENTALIS LEAF	6 [hp_X]/59mL
ACONITUM NAPELLUS WHOLE	6 [hp_X]/59mL
POTASSIUM ALUM	6 [hp_X]/59mL
SILICON DIOXIDE	100 [hp_X]/59mL
ANHYDROUS DIBASIC CALCIUM PHOSPHATE	12 [hp_X]/59mL
ALLYLTHIOUREA	60 [hp_X]/59mL
NITRIC ACID	8 [hp_X]/59mL
GRAPHITE	6 [hp_X]/59mL
LACTOSE, X-RAY EXPOSED (1000 RAD)	6 [hp_X]/59mL
ARNICA MONTANA WHOLE	3 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
0T0DQN8786	Internal UNII lookup
U0NQ8555JD	Internal UNII lookup
1L24V9R23S	Internal UNII lookup
ETJ7Z6XBU4	Internal UNII lookup
L11K75P92J	Internal UNII lookup
706IDJ14B7	Internal UNII lookup
411VRN1TV4	Internal UNII lookup
4QQN74LH4O	Internal UNII lookup
LNT739I158	Internal UNII lookup
O80TY208ZW	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ad0e9159-ed68-48aa-a7d1-7ff5c32ec304	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2026-01-09	C84
2026-01-09	C84
2024-01-30	C84
2024-01-30	C84

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63083-2084-2	Anti-Scar Drops2084	59 mL in 1 BOTTLE, DROPPER	LIQUID	59		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63083-2084	ANTI-SCAR DROPS 2084 (ANTI-SCAR DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]	1	Current NDC, Legacy NDC, 1 package rows	20220215_ad0e9159-ed68-48aa-a7d1-7ff5c32ec304.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Anti-Scar Drops 2084	ANTI-SCAR DROPS	Professional Complementary Health Formulas	ad0e9159-ed68-48aa-a7d1-7ff5c32ec304	2026-01-08	Warnings	Exact identifier ndc (package): 63083-2084-2 ndc (product): 63083-2084 ndc11 (package): 63083208402

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
706IDJ14B7	ALLYLTHIOUREA	109-57-9	ALLYLTHIOUREA
L11K75P92J	ANHYDROUS DIBASIC CALCIUM PHOSPHATE	7757-93-9	ANHYDROUS DIBASIC CALCIUM PHOSPHATE
4QQN74LH4O	GRAPHITE	7782-42-5	GRAPHITE
LNT739I158	LACTOSE, X-RAY EXPOSED (1000 RAD)		LACTOSE, X-RAY EXPOSED (1000 RAD)
411VRN1TV4	NITRIC ACID	7697-37-2	NITRIC ACID
1L24V9R23S	POTASSIUM ALUM	7784-24-9	POTASSIUM ALUM
ETJ7Z6XBU4	SILICON DIOXIDE	7631-86-9	SILICON DIOXIDE
0T0DQN8786	THUJA OCCIDENTALIS LEAF		THUJA OCCIDENTALIS LEAF

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63083-2084-2	63083208402	59 mL in 1 BOTTLE, DROPPER (63083-2084-2)	59 ml	1985-08-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
C84	Professional Complementary Health Formulas \| Natural Pharmaceutical Manufacturing LLC	2026-01-08	HUMAN OTC DRUG LABEL	2